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rs137853932

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853932(A;A)
Make rs137853932(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position18599564
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853932
ebirs137853932
HLIrs137853932
Exacrs137853932
Varsomers137853932
Maprs137853932
PheGenIrs137853932
hapmaprs137853932
1000 genomesrs137853932
hgdprs137853932
ensemblrs137853932
gopubmedrs137853932
geneviewrs137853932
scholarrs137853932
googlers137853932
pharmgkbrs137853932
gwascentralrs137853932
openSNPrs137853932
23andMers137853932
23andMe allrs137853932
SNP Nexus

SNPshotrs137853932
SNPdbers137853932
MSV3drs137853932
GWAS Ctlgrs137853932
Max Magnitude0
ClinVar
Risk rs137853932(A;A)
Alt rs137853932(A;A)
Reference rs137853932(G;G)
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.18710374C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020617.1,


OMIM272430
Desc
Variant
Relatedalso