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rs794728016

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728016(G;G)
Make rs794728016(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position116763206
GeneMET
is asnp
is mentioned by
dbSNPrs794728016
ebirs794728016
HLIrs794728016
Exacrs794728016
Varsomers794728016
Maprs794728016
PheGenIrs794728016
hapmaprs794728016
1000 genomesrs794728016
hgdprs794728016
ensemblrs794728016
gopubmedrs794728016
geneviewrs794728016
scholarrs794728016
googlers794728016
pharmgkbrs794728016
gwascentralrs794728016
openSNPrs794728016
23andMers794728016
23andMe allrs794728016
SNP Nexus

SNPshotrs794728016
SNPdbers794728016
MSV3drs794728016
GWAS Ctlgrs794728016
Max Magnitude0
ClinVar
Risk rs794728016(G;G)
Alt rs794728016(G;G)
Reference rs794728016(T;T)
Significance Pathogenic
Disease Nonsyndromic Hearing Loss and Deafness Deafness
Variation info
Gene MET
CLNDBN Nonsyndromic Hearing Loss and Deafness, Autosomal Recessive Deafness, autosomal recessive 97
Reversed 0
HGVS NC_000007.13:g.116403260T>G
CLNSRC OMIM Allelic Variant University of the Punjab
CLNACC RCV000185580.2, RCV000202585.2,