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rs137853926

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853926(C;T)
Make rs137853926(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18598591
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853926
ebirs137853926
HLIrs137853926
Exacrs137853926
Varsomers137853926
Maprs137853926
PheGenIrs137853926
hapmaprs137853926
1000 genomesrs137853926
hgdprs137853926
ensemblrs137853926
gopubmedrs137853926
geneviewrs137853926
scholarrs137853926
googlers137853926
pharmgkbrs137853926
gwascentralrs137853926
openSNPrs137853926
23andMers137853926
23andMe allrs137853926
SNP Nexus

SNPshotrs137853926
SNPdbers137853926
MSV3drs137853926
GWAS Ctlgrs137853926
Max Magnitude0
ClinVar
Risk rs137853926(T;T)
Alt rs137853926(T;T)
Reference rs137853926(C;C)
Significance Pathogenic
Disease Cold-induced sweating syndrome 1
Variation info
Gene CRLF1
CLNDBN Cold-induced sweating syndrome 1
Reversed 1
HGVS NC_000019.9:g.18709401G>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020619.1,


OMIM272430
Desc
Variant
Relatedalso