chr18:60228805:G>A Detail (hg38)

Information

Genome

Assembly Position
hg19 chr18:57,896,038-57,896,038 View the variant detail on this assembly version.
hg38 chr18:60,228,805-60,228,805

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
0.029 Diabetes Mellitus, Non-Insulin-Dependent We examined rs17782313, rs17700633, rs12970134, rs477181, rs502933, and rs445050... BeFree 19073769 Detail
Annotation

Annotations

DescrptionSourceLinks
We examined rs17782313, rs17700633, rs12970134, rs477181, rs502933, and rs4450508 near MC4R for asso... DisGeNET Detail
Gene
-
dbSNP
rs477181 dbSNP
Genome
hg38
Position
chr18:60,228,805-60,228,805
Variant Type
snv
Reference Allele
G
Alternative Allele
A
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