rs769664228
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(I;I) | 0 | common genotype |
Make rs769664228(-;-) |
Make rs769664228(-;CGGCAGCCAGGACCTGGGGGCTGAATG) |
Make rs769664228(CGGCAGCCAGGACCTGGGGGCTGAATG;CGGCAGCCAGGACCTGGGGGCTGAATG) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 44258043 |
Gene | SLC4A1 |
is a | snp |
is | mentioned by |
dbSNP | rs769664228 |
dbSNP (classic) | rs769664228 |
ClinGen | rs769664228 |
ebi | rs769664228 |
HLI | rs769664228 |
Exac | rs769664228 |
Gnomad | rs769664228 |
Varsome | rs769664228 |
LitVar | rs769664228 |
Map | rs769664228 |
PheGenI | rs769664228 |
Biobank | rs769664228 |
1000 genomes | rs769664228 |
hgdp | rs769664228 |
ensembl | rs769664228 |
geneview | rs769664228 |
scholar | rs769664228 |
rs769664228 | |
pharmgkb | rs769664228 |
gwascentral | rs769664228 |
openSNP | rs769664228 |
23andMe | rs769664228 |
SNPshot | rs769664228 |
SNPdbe | rs769664228 |
MSV3d | rs769664228 |
GWAS Ctlg | rs769664228 |
Max Magnitude | 0 |
aka NM_000342.3(SLC4A1):c.1199_1225del27 or (p.Ala400_Ala408del)
OMIM pathogenic variant