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rs267607037

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607037(G;T)
Make rs267607037(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position2948696
GeneSERPINB6
is asnp
is mentioned by
dbSNPrs267607037
ebirs267607037
HLIrs267607037
Exacrs267607037
Varsomers267607037
Maprs267607037
PheGenIrs267607037
hapmaprs267607037
1000 genomesrs267607037
hgdprs267607037
ensemblrs267607037
gopubmedrs267607037
geneviewrs267607037
scholarrs267607037
googlers267607037
pharmgkbrs267607037
gwascentralrs267607037
openSNPrs267607037
23andMers267607037
23andMe allrs267607037
SNP Nexus

SNPshotrs267607037
SNPdbers267607037
MSV3drs267607037
GWAS Ctlgrs267607037
Max Magnitude0
ClinVar
Risk rs267607037(T;T)
Alt rs267607037(T;T)
Reference rs267607037(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene SERPINB6
CLNDBN Deafness, autosomal recessive 91
Reversed 1
HGVS NC_000006.11:g.2948930C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014571.26,