chr6:31563533:T>G Detail (hg38)

Information

Genome

Assembly Position
hg19 chr6:31,531,310-31,531,310 View the variant detail on this assembly version.
hg38 chr6:31,563,533-31,563,533

HGVS

[No Data.]
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
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.012 Diabetes Mellitus, Insulin-Dependent Markers rs4151659 (mapping to CFB) and rs7762619 (mapping 5' of LTA) were the mo... BeFree 20054343 Detail
Annotation

Annotations

DescrptionSourceLinks
Markers rs4151659 (mapping to CFB) and rs7762619 (mapping 5' of LTA) were the most strongly associat... DisGeNET Detail
Gene
-
dbSNP
rs7762619 dbSNP
Genome
hg38
Position
chr6:31,563,533-31,563,533
Variant Type
snv
Reference Allele
T
Alternative Allele
G
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