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rs869320674

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320674(-;-)
Make rs869320674(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position114403335
GeneWHRN
is asnp
is mentioned by
dbSNPrs869320674
ebirs869320674
HLIrs869320674
Exacrs869320674
Varsomers869320674
Maprs869320674
PheGenIrs869320674
hapmaprs869320674
1000 genomesrs869320674
hgdprs869320674
ensemblrs869320674
gopubmedrs869320674
geneviewrs869320674
scholarrs869320674
googlers869320674
pharmgkbrs869320674
gwascentralrs869320674
openSNPrs869320674
23andMers869320674
23andMe allrs869320674
SNP Nexus

SNPshotrs869320674
SNPdbers869320674
MSV3drs869320674
GWAS Ctlgrs869320674
Max Magnitude0
ClinVar
Risk rs869320674(;)
Alt rs869320674(;)
Reference rs869320674(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene DFNB31
CLNDBN Deafness, autosomal recessive 31
Reversed 1
HGVS NC_000009.11:g.117165615delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000190401.2,