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rs137853927

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853927(G;T)
Make rs137853927(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18596895
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853927
ebirs137853927
HLIrs137853927
Exacrs137853927
Varsomers137853927
Maprs137853927
PheGenIrs137853927
hapmaprs137853927
1000 genomesrs137853927
hgdprs137853927
ensemblrs137853927
gopubmedrs137853927
geneviewrs137853927
scholarrs137853927
googlers137853927
pharmgkbrs137853927
gwascentralrs137853927
openSNPrs137853927
23andMers137853927
23andMe allrs137853927
SNP Nexus

SNPshotrs137853927
SNPdbers137853927
MSV3drs137853927
GWAS Ctlgrs137853927
Max Magnitude0
ClinVar
Risk rs137853927(T;T)
Alt rs137853927(T;T)
Reference rs137853927(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.18707705C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000020621.1,


OMIM272430
Desc
Variant
Relatedalso