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rs756000896

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs756000896(A;A)
Make rs756000896(A;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position71223989
GeneGJB1
is asnp
is mentioned by
dbSNPrs756000896
ebirs756000896
HLIrs756000896
Exacrs756000896
Varsomers756000896
Maprs756000896
PheGenIrs756000896
hapmaprs756000896
1000 genomesrs756000896
hgdprs756000896
ensemblrs756000896
gopubmedrs756000896
geneviewrs756000896
scholarrs756000896
googlers756000896
pharmgkbrs756000896
gwascentralrs756000896
openSNPrs756000896
23andMers756000896
23andMe allrs756000896
SNP Nexus

SNPshotrs756000896
SNPdbers756000896
MSV3drs756000896
GWAS Ctlgrs756000896
Max Magnitude0
ClinVar
Risk rs756000896(A,T;A,T)
Alt rs756000896(A,T;A,T)
Reference rs756000896(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GJB1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.70443839C>A
CLNSRC
CLNACC RCV000236380.1,