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rs137853928

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs137853928(-;-)
Make rs137853928(-;GT)
Make rs137853928(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome19
Position18596902
GeneCRLF1
is asnp
is mentioned by
dbSNPrs137853928
ebirs137853928
HLIrs137853928
Exacrs137853928
Varsomers137853928
Maprs137853928
PheGenIrs137853928
hapmaprs137853928
1000 genomesrs137853928
hgdprs137853928
ensemblrs137853928
gopubmedrs137853928
geneviewrs137853928
scholarrs137853928
googlers137853928
pharmgkbrs137853928
gwascentralrs137853928
openSNPrs137853928
23andMers137853928
23andMe allrs137853928
SNP Nexus

SNPshotrs137853928
SNPdbers137853928
MSV3drs137853928
GWAS Ctlgrs137853928
Max Magnitude0
OMIM604237
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853928(;)
Alt rs137853928(;)
Reference rs137853928(TG;TG)
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.18707711_18707712delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000210224.2,