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rs137853145

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137853145(C;T)
Make rs137853145(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18596918
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853145
ebirs137853145
HLIrs137853145
Exacrs137853145
Varsomers137853145
Maprs137853145
PheGenIrs137853145
hapmaprs137853145
1000 genomesrs137853145
hgdprs137853145
ensemblrs137853145
gopubmedrs137853145
geneviewrs137853145
scholarrs137853145
googlers137853145
pharmgkbrs137853145
gwascentralrs137853145
openSNPrs137853145
23andMers137853145
23andMe allrs137853145
SNP Nexus

SNPshotrs137853145
SNPdbers137853145
MSV3drs137853145
GWAS Ctlgrs137853145
Max Magnitude0
OMIM604237
Desc
Variant0009
Relatedalso
ClinVar
Risk rs137853145(G,T;G,T)
Alt rs137853145(G,T;G,T)
Reference rs137853145(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.18707728G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006067.3,