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rs137853144

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853144(A;T)
Make rs137853144(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position18594357
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853144
ebirs137853144
HLIrs137853144
Exacrs137853144
Varsomers137853144
Maprs137853144
PheGenIrs137853144
hapmaprs137853144
1000 genomesrs137853144
hgdprs137853144
ensemblrs137853144
gopubmedrs137853144
geneviewrs137853144
scholarrs137853144
googlers137853144
pharmgkbrs137853144
gwascentralrs137853144
openSNPrs137853144
23andMers137853144
23andMe allrs137853144
SNP Nexus

SNPshotrs137853144
SNPdbers137853144
MSV3drs137853144
GWAS Ctlgrs137853144
Max Magnitude0
OMIM604237
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137853144(T;T)
Alt rs137853144(T;T)
Reference rs137853144(A;A)
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.18705167T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000006065.3,