Have questions? Visit https://www.reddit.com/r/SNPedia

rs201306709

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201306709(A;A)
Make rs201306709(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position65368997
GeneMSRB3
is asnp
is mentioned by
dbSNPrs201306709
ebirs201306709
HLIrs201306709
Exacrs201306709
Varsomers201306709
Maprs201306709
PheGenIrs201306709
hapmaprs201306709
1000 genomesrs201306709
hgdprs201306709
ensemblrs201306709
gopubmedrs201306709
geneviewrs201306709
scholarrs201306709
googlers201306709
pharmgkbrs201306709
gwascentralrs201306709
openSNPrs201306709
23andMers201306709
23andMe allrs201306709
SNP Nexus

SNPshotrs201306709
SNPdbers201306709
MSV3drs201306709
GWAS Ctlgrs201306709
Max Magnitude0
ClinVar
Risk rs201306709(A;A)
Alt rs201306709(A;A)
Reference rs201306709(G;G)
Significance Probable-Pathogenic
Disease Non-syndromic genetic deafness
Variation info
Gene MSRB3
CLNDBN Non-syndromic genetic deafness
Reversed 0
HGVS NC_000012.11:g.65762777G>A
CLNSRC
CLNACC RCV000216815.1,