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rs137853935

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853935(C;C)
Make rs137853935(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position67365138
GeneCLCF1, HSD17B12
is asnp
is mentioned by
dbSNPrs137853935
ebirs137853935
HLIrs137853935
Exacrs137853935
Varsomers137853935
Maprs137853935
PheGenIrs137853935
hapmaprs137853935
1000 genomesrs137853935
hgdprs137853935
ensemblrs137853935
gopubmedrs137853935
geneviewrs137853935
scholarrs137853935
googlers137853935
pharmgkbrs137853935
gwascentralrs137853935
openSNPrs137853935
23andMers137853935
23andMe allrs137853935
SNP Nexus

SNPshotrs137853935
SNPdbers137853935
MSV3drs137853935
GWAS Ctlgrs137853935
Max Magnitude0
ClinVar
Risk rs137853935(C;C)
Alt rs137853935(C;C)
Reference rs137853935(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.67132609A>G
CLNSRC ClinVar GeneReviews
CLNACC RCV000020693.1,