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rs137853934

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853934(C;C)
Make rs137853934(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67367597
GeneCLCF1, HSD17B12
is asnp
is mentioned by
dbSNPrs137853934
ebirs137853934
HLIrs137853934
Exacrs137853934
Varsomers137853934
Maprs137853934
PheGenIrs137853934
hapmaprs137853934
1000 genomesrs137853934
hgdprs137853934
ensemblrs137853934
gopubmedrs137853934
geneviewrs137853934
scholarrs137853934
googlers137853934
pharmgkbrs137853934
gwascentralrs137853934
openSNPrs137853934
23andMers137853934
23andMe allrs137853934
SNP Nexus

SNPshotrs137853934
SNPdbers137853934
MSV3drs137853934
GWAS Ctlgrs137853934
Max Magnitude0
ClinVar
Risk rs137853934(C;C)
Alt rs137853934(C;C)
Reference rs137853934(T;T)
Significance Pathogenic
Disease Cold-induced sweating syndrome 2
Variation info
Gene CLCF1 LOC100130987
CLNDBN Cold-induced sweating syndrome 2
Reversed 1
HGVS NC_000011.9:g.67135068A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020692.1,