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rs137853931

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853931(-;-)
Make rs137853931(-;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position18599659
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853931
ebirs137853931
HLIrs137853931
Exacrs137853931
Varsomers137853931
Maprs137853931
PheGenIrs137853931
hapmaprs137853931
1000 genomesrs137853931
hgdprs137853931
ensemblrs137853931
gopubmedrs137853931
geneviewrs137853931
scholarrs137853931
googlers137853931
pharmgkbrs137853931
gwascentralrs137853931
openSNPrs137853931
23andMers137853931
23andMe allrs137853931
SNP Nexus

SNPshotrs137853931
SNPdbers137853931
MSV3drs137853931
GWAS Ctlgrs137853931
Max Magnitude0
ClinVar
Risk rs137853931(;)
Alt rs137853931(;)
Reference rs137853931(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.18710469delG
CLNSRC ClinVar GeneReviews
CLNACC RCV000020615.1,


OMIM272430
Desc
Variant
Relatedalso