rs869312035
From SNPedia
Merged into | rs137853928 |
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs869312035(-;-) |
Make rs869312035(-;TG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 19 |
Position | 18596901 |
Gene | CRLF1 |
is a | snp |
is | mentioned by |
dbSNP | rs869312035 |
dbSNP (classic) | rs869312035 |
ClinGen | rs869312035 |
ebi | rs869312035 |
HLI | rs869312035 |
Exac | rs869312035 |
Gnomad | rs869312035 |
Varsome | rs869312035 |
LitVar | rs869312035 |
Map | rs869312035 |
PheGenI | rs869312035 |
Biobank | rs869312035 |
1000 genomes | rs869312035 |
hgdp | rs869312035 |
ensembl | rs869312035 |
geneview | rs869312035 |
scholar | rs869312035 |
rs869312035 | |
pharmgkb | rs869312035 |
gwascentral | rs869312035 |
openSNP | rs869312035 |
23andMe | rs869312035 |
SNPshot | rs869312035 |
SNPdbe | rs869312035 |
MSV3d | rs869312035 |
GWAS Ctlg | rs869312035 |
Status | Merged into rs137853928 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
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, |