rs75731670
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs75731670(C;T) |
Make rs75731670(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 44254581 |
Gene | SLC4A1 |
is a | snp |
is | mentioned by |
dbSNP | rs75731670 |
dbSNP (classic) | rs75731670 |
ClinGen | rs75731670 |
ebi | rs75731670 |
HLI | rs75731670 |
Exac | rs75731670 |
Gnomad | rs75731670 |
Varsome | rs75731670 |
LitVar | rs75731670 |
Map | rs75731670 |
PheGenI | rs75731670 |
Biobank | rs75731670 |
1000 genomes | rs75731670 |
hgdp | rs75731670 |
ensembl | rs75731670 |
geneview | rs75731670 |
scholar | rs75731670 |
rs75731670 | |
pharmgkb | rs75731670 |
gwascentral | rs75731670 |
openSNP | rs75731670 |
23andMe | rs75731670 |
SNPshot | rs75731670 |
SNPdbe | rs75731670 |
MSV3d | rs75731670 |
GWAS Ctlg | rs75731670 |
Merged from | Rs121912740 |
GMAF | 0.0 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs75731670(G;G) rs75731670(T;T) |
Alt | rs75731670(G;G) rs75731670(T;T) |
Reference | Rs75731670(C;C) |
Significance | Other |
Disease | BLOOD GROUP--WRIGHT ANTIGEN |
Variation | info |
Gene | SLC4A1 |
CLNDBN | BLOOD GROUP--WRIGHT ANTIGEN |
Reversed | 0 |
HGVS | NC_000017.10:g.42331949C>T |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000019336.28, |