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

rs778909195

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs778909195(A;A)
Make rs778909195(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position43604020
GeneSTRC
is asnp
is mentioned by
dbSNPrs778909195
ebirs778909195
HLIrs778909195
Exacrs778909195
Varsomers778909195
Maprs778909195
PheGenIrs778909195
hapmaprs778909195
1000 genomesrs778909195
hgdprs778909195
ensemblrs778909195
gopubmedrs778909195
geneviewrs778909195
scholarrs778909195
googlers778909195
pharmgkbrs778909195
gwascentralrs778909195
openSNPrs778909195
23andMers778909195
23andMe allrs778909195
SNP Nexus

SNPshotrs778909195
SNPdbers778909195
MSV3drs778909195
GWAS Ctlgrs778909195
Max Magnitude0
ClinVar
Risk rs778909195(A;A)
Alt rs778909195(A;A)
Reference rs778909195(G;G)
Significance Probable-Pathogenic
Disease Deafness
Variation info
Gene STRC
CLNDBN Deafness, autosomal recessive 16
Reversed 0
HGVS NC_000015.9:g.43896218G>A
CLNSRC
CLNACC RCV000193949.1,