rs141686175
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs141686175(A;G) |
Make rs141686175(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 38872215 |
Gene | SCN11A |
is a | snp |
is | mentioned by |
dbSNP | rs141686175 |
dbSNP (classic) | rs141686175 |
ClinGen | rs141686175 |
ebi | rs141686175 |
HLI | rs141686175 |
Exac | rs141686175 |
Gnomad | rs141686175 |
Varsome | rs141686175 |
LitVar | rs141686175 |
Map | rs141686175 |
PheGenI | rs141686175 |
Biobank | rs141686175 |
1000 genomes | rs141686175 |
hgdp | rs141686175 |
ensembl | rs141686175 |
geneview | rs141686175 |
scholar | rs141686175 |
rs141686175 | |
pharmgkb | rs141686175 |
gwascentral | rs141686175 |
openSNP | rs141686175 |
23andMe | rs141686175 |
SNPshot | rs141686175 |
SNPdbe | rs141686175 |
MSV3d | rs141686175 |
GWAS Ctlg | rs141686175 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141686175(G;G) |
Alt | rs141686175(G;G) |
Reference | Rs141686175(A;A) |
Significance | Pathogenic |
Disease | Episodic pain syndrome not specified |
Variation | info |
Gene | SCN11A |
CLNDBN | Episodic pain syndrome, familial, 3 not specified |
Reversed | 0 |
HGVS | NC_000003.11:g.38913706A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000144934.3, RCV000282888.1, |