Have questions? Visit https://www.reddit.com/r/SNPedia

rs869312035

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs869312035(-;-)
Make rs869312035(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position18596901
GeneCRLF1
is asnp
is mentioned by
dbSNPrs869312035
ebirs869312035
HLIrs869312035
Exacrs869312035
Varsomers869312035
Maprs869312035
PheGenIrs869312035
hapmaprs869312035
1000 genomesrs869312035
hgdprs869312035
ensemblrs869312035
gopubmedrs869312035
geneviewrs869312035
scholarrs869312035
googlers869312035
pharmgkbrs869312035
gwascentralrs869312035
openSNPrs869312035
23andMers869312035
23andMe allrs869312035
SNP Nexus

SNPshotrs869312035
SNPdbers869312035
MSV3drs869312035
GWAS Ctlgrs869312035
Max Magnitude0
ClinVar
Risk rs869312035(;)
Alt rs869312035(;)
Reference rs869312035(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,