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rs137853933

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853933(A;A)
Make rs137853933(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position18596711
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853933
ebirs137853933
HLIrs137853933
Exacrs137853933
Varsomers137853933
Maprs137853933
PheGenIrs137853933
hapmaprs137853933
1000 genomesrs137853933
hgdprs137853933
ensemblrs137853933
gopubmedrs137853933
geneviewrs137853933
scholarrs137853933
googlers137853933
pharmgkbrs137853933
gwascentralrs137853933
openSNPrs137853933
23andMers137853933
23andMe allrs137853933
SNP Nexus

SNPshotrs137853933
SNPdbers137853933
MSV3drs137853933
GWAS Ctlgrs137853933
Max Magnitude0
ClinVar
Risk rs137853933(A,T;A,T)
Alt rs137853933(A,T;A,T)
Reference rs137853933(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.18707521C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000020622.1,


OMIM272430
Desc
Variant
Relatedalso