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rs137853235

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853235(A;A)
Make rs137853235(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position81752250
GeneHGF
is asnp
is mentioned by
dbSNPrs137853235
ebirs137853235
HLIrs137853235
Exacrs137853235
Varsomers137853235
Maprs137853235
PheGenIrs137853235
hapmaprs137853235
1000 genomesrs137853235
hgdprs137853235
ensemblrs137853235
gopubmedrs137853235
geneviewrs137853235
scholarrs137853235
googlers137853235
pharmgkbrs137853235
gwascentralrs137853235
openSNPrs137853235
23andMers137853235
23andMe allrs137853235
SNP Nexus

SNPshotrs137853235
SNPdbers137853235
MSV3drs137853235
GWAS Ctlgrs137853235
Max Magnitude0
OMIM142409
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853235(A;A)
Alt rs137853235(A;A)
Reference rs137853235(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene HGF
CLNDBN Deafness, autosomal recessive 39
Reversed 1
HGVS NC_000007.13:g.81381566C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016089.22,