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rs768727082

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs768727082(-;G)
Make rs768727082(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position18597033
GeneCRLF1
is asnp
is mentioned by
dbSNPrs768727082
ClinGenrs768727082
ebirs768727082
HLIrs768727082
Exacrs768727082
Varsomers768727082
Maprs768727082
PheGenIrs768727082
hapmaprs768727082
1000 genomesrs768727082
hgdprs768727082
ensemblrs768727082
gopubmedrs768727082
geneviewrs768727082
scholarrs768727082
googlers768727082
pharmgkbrs768727082
gwascentralrs768727082
openSNPrs768727082
23andMers768727082
23andMe allrs768727082
SNP Nexus

SNPshotrs768727082
SNPdbers768727082
MSV3drs768727082
GWAS Ctlgrs768727082
Max Magnitude0
ClinVar
Risk rs768727082(G;G)
Alt rs768727082(G;G)
Reference Rs768727082(-;-)
Significance Pathogenic
Disease Cold-induced sweating syndrome 1
Variation info
Gene CRLF1
CLNDBN Cold-induced sweating syndrome 1
Reversed 0
HGVS NC_000019.9:g.18707844dupG
CLNSRC
CLNACC RCV000195773.1,