chr10:17841064:G>A Detail (hg38) (MRC1)

Information

Genome

Assembly Position
hg19 chr10:18,129,993-18,129,993 View the variant detail on this assembly version.
hg38 chr10:17,841,064-17,841,064

HGVS

Type Transcript Protein
RefSeq
Ensemble ENST00000569591.3:c.916+258G>A
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 153618 OMIM
HGNC 7228 HGNC
Ensembl ENSG00000260314 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv38551101 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 Leprosy, Multibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
<0.001 Leprosy, Multibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
<0.001 Leprosy, Paucibacillary However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) ... BeFree 22392581 Detail
Annotation

Annotations

DescrptionSourceLinks
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail
However, we found that variants rs692527 (P = 0.022) and rs34856358 (P = 0.022) of the MRC1 gene wer... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs692527 dbSNP
Genome
hg38
Position
chr10:17,841,064-17,841,064
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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