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rs104894198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894198(A;A)
Make rs104894198(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position67365493
GeneCLCF1, HSD17B12
is asnp
is mentioned by
dbSNPrs104894198
ebirs104894198
HLIrs104894198
Exacrs104894198
Varsomers104894198
Maprs104894198
PheGenIrs104894198
hapmaprs104894198
1000 genomesrs104894198
hgdprs104894198
ensemblrs104894198
gopubmedrs104894198
geneviewrs104894198
scholarrs104894198
googlers104894198
pharmgkbrs104894198
gwascentralrs104894198
openSNPrs104894198
23andMers104894198
23andMe allrs104894198
SNP Nexus

SNPshotrs104894198
SNPdbers104894198
MSV3drs104894198
GWAS Ctlgrs104894198
Max Magnitude0
OMIM607672
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104894198(A,T;A,T)
Alt rs104894198(A,T;A,T)
Reference rs104894198(C;C)
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.67132964G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003064.2,