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rs104894670

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs104894670(A;A)
Make rs104894670(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position18599720
GeneCRLF1
is asnp
is mentioned by
dbSNPrs104894670
ebirs104894670
HLIrs104894670
Exacrs104894670
Varsomers104894670
Maprs104894670
PheGenIrs104894670
hapmaprs104894670
1000 genomesrs104894670
hgdprs104894670
ensemblrs104894670
gopubmedrs104894670
geneviewrs104894670
scholarrs104894670
googlers104894670
pharmgkbrs104894670
gwascentralrs104894670
openSNPrs104894670
23andMers104894670
23andMe allrs104894670
SNP Nexus

SNPshotrs104894670
SNPdbers104894670
MSV3drs104894670
GWAS Ctlgrs104894670
Max Magnitude0
OMIM604237
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894670(A;A)
Alt rs104894670(A;A)
Reference rs104894670(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.18710530C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006060.3, RCV000020614.1,