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rs148438059

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148438059(C;T)
Make rs148438059(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position63327234
GeneCA12, LOC105370859
is asnp
is mentioned by
dbSNPrs148438059
ebirs148438059
HLIrs148438059
Exacrs148438059
Varsomers148438059
Maprs148438059
PheGenIrs148438059
hapmaprs148438059
1000 genomesrs148438059
hgdprs148438059
ensemblrs148438059
gopubmedrs148438059
geneviewrs148438059
scholarrs148438059
googlers148438059
pharmgkbrs148438059
gwascentralrs148438059
openSNPrs148438059
23andMers148438059
23andMe allrs148438059
SNP Nexus

SNPshotrs148438059
SNPdbers148438059
MSV3drs148438059
GWAS Ctlgrs148438059
Max Magnitude0
ClinVar
Risk rs148438059(T;T)
Alt rs148438059(T;T)
Reference rs148438059(C;C)
Significance Pathogenic
Disease Hyperchlorhidrosis
Variation info
Gene CA12
CLNDBN Hyperchlorhidrosis, isolated
Reversed 0
HGVS NC_000015.9:g.63619433C>T
CLNSRC
CLNACC RCV000236291.1,