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rs875989828

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs875989828(A;A)
Make rs875989828(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position24873800
GeneFAM65B
is asnp
is mentioned by
dbSNPrs875989828
ebirs875989828
HLIrs875989828
Exacrs875989828
Varsomers875989828
Maprs875989828
PheGenIrs875989828
hapmaprs875989828
1000 genomesrs875989828
hgdprs875989828
ensemblrs875989828
gopubmedrs875989828
geneviewrs875989828
scholarrs875989828
googlers875989828
pharmgkbrs875989828
gwascentralrs875989828
openSNPrs875989828
23andMers875989828
23andMe allrs875989828
SNP Nexus

SNPshotrs875989828
SNPdbers875989828
MSV3drs875989828
GWAS Ctlgrs875989828
Max Magnitude0
ClinVar
Risk rs875989828(A;A)
Alt rs875989828(A;A)
Reference rs875989828(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene FAM65B
CLNDBN Deafness, autosomal recessive 104
Reversed 1
HGVS NC_000006.11:g.24874028C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000190353.2,