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rs74315438

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315438(A;A)
Make rs74315438(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position36461395
GeneCLDN14
is asnp
is mentioned by
dbSNPrs74315438
ebirs74315438
HLIrs74315438
Exacrs74315438
Varsomers74315438
Maprs74315438
PheGenIrs74315438
hapmaprs74315438
1000 genomesrs74315438
hgdprs74315438
ensemblrs74315438
gopubmedrs74315438
geneviewrs74315438
scholarrs74315438
googlers74315438
pharmgkbrs74315438
gwascentralrs74315438
openSNPrs74315438
23andMers74315438
23andMe allrs74315438
SNP Nexus

SNPshotrs74315438
SNPdbers74315438
MSV3drs74315438
GWAS Ctlgrs74315438
Max Magnitude0
OMIM605608
Desc
Variant0003
Relatedalso
ClinVar
Risk rs74315438(A;A)
Alt rs74315438(A;A)
Reference rs74315438(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene CLDN14
CLNDBN Deafness, autosomal recessive 29
Reversed 1
HGVS NC_000021.8:g.37833693C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005125.3,