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rs775067652

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs775067652(G;T)
Make rs775067652(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position63345543
GeneCA12, LOC105370859
is asnp
is mentioned by
dbSNPrs775067652
ebirs775067652
HLIrs775067652
Exacrs775067652
Varsomers775067652
Maprs775067652
PheGenIrs775067652
hapmaprs775067652
1000 genomesrs775067652
hgdprs775067652
ensemblrs775067652
gopubmedrs775067652
geneviewrs775067652
scholarrs775067652
googlers775067652
pharmgkbrs775067652
gwascentralrs775067652
openSNPrs775067652
23andMers775067652
23andMe allrs775067652
SNP Nexus

SNPshotrs775067652
SNPdbers775067652
MSV3drs775067652
GWAS Ctlgrs775067652
Max Magnitude0
ClinVar
Risk rs775067652(T;T)
Alt rs775067652(T;T)
Reference rs775067652(G;G)
Significance Pathogenic
Disease Hyperchlorhidrosis
Variation info
Gene CA12
CLNDBN Hyperchlorhidrosis, isolated
Reversed 0
HGVS NC_000015.9:g.63637742G>T
CLNSRC
CLNACC RCV000235472.1,