chr7:140690777:> Detail (hg38)

Information

Genome

Assembly Position
hg19 chr7:140,390,577-140,422,590 
hg38 chr7:140,690,777-140,722,790

HGVS

Type Transcript Protein
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

[No Data.]

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
<0.001 Graves Disease NA BeFree Detail
<0.001 hepatitis B NA BeFree Detail
<0.001 carpal tunnel syndrome One hundred and three self-reported coloured participants, with a history of car... BeFree 24966028 Detail
0.003 ischemia NA LHGDN Detail
0.003 Reperfusion Injury NA LHGDN Detail
<0.001 schistosomiasis NA BeFree Detail
<0.001 Precocious pubarche NA BeFree Detail
0.003 Malignant neoplasm of prostate NA BeFree,GAD Detail
<0.001 prostate carcinoma NA BeFree Detail
<0.001 liver carcinoma NA BeFree Detail
Annotation

Annotations

DescrptionSourceLinks
NA DisGeNET Detail
NA DisGeNET Detail
One hundred and three self-reported coloured participants, with a history of carpal tunnel release s... DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail
NA DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs14774622 dbSNP
Genome
hg38
Position
chr7:140,690,777-140,722,790
Variant Type
snv
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