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rs137853143

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137853143(G;G)
Make rs137853143(G;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18599736
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853143
ebirs137853143
HLIrs137853143
Exacrs137853143
Varsomers137853143
Maprs137853143
PheGenIrs137853143
hapmaprs137853143
1000 genomesrs137853143
hgdprs137853143
ensemblrs137853143
gopubmedrs137853143
geneviewrs137853143
scholarrs137853143
googlers137853143
pharmgkbrs137853143
gwascentralrs137853143
openSNPrs137853143
23andMers137853143
23andMe allrs137853143
SNP Nexus

SNPshotrs137853143
SNPdbers137853143
MSV3drs137853143
GWAS Ctlgrs137853143
Max Magnitude0
OMIM604237
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853143(G;G)
Alt rs137853143(G;G)
Reference rs137853143(T;T)
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.18710546A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000006062.3,