rs28938168
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs28938168(A;A) |
Make rs28938168(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 117822424 |
Gene | FXYD2, FXYD6-FXYD2 |
is a | snp |
is | mentioned by |
dbSNP | rs28938168 |
dbSNP (classic) | rs28938168 |
ClinGen | rs28938168 |
ebi | rs28938168 |
HLI | rs28938168 |
Exac | rs28938168 |
Gnomad | rs28938168 |
Varsome | rs28938168 |
LitVar | rs28938168 |
Map | rs28938168 |
PheGenI | rs28938168 |
Biobank | rs28938168 |
1000 genomes | rs28938168 |
hgdp | rs28938168 |
ensembl | rs28938168 |
geneview | rs28938168 |
scholar | rs28938168 |
rs28938168 | |
pharmgkb | rs28938168 |
gwascentral | rs28938168 |
openSNP | rs28938168 |
23andMe | rs28938168 |
SNPshot | rs28938168 |
SNPdbe | rs28938168 |
MSV3d | rs28938168 |
GWAS Ctlg | rs28938168 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs28938168(A;A) |
Alt | rs28938168(A;A) |
Reference | Rs28938168(G;G) |
Significance | Pathogenic |
Disease | Hypomagnesemia 2 |
Variation | info |
Gene | FXYD2 FXYD6-FXYD2 |
CLNDBN | Hypomagnesemia 2, renal |
Reversed | 1 |
HGVS | NC_000011.9:g.117693139C>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000008123.3, |