rs1363364
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1363364(A;A) |
Make rs1363364(A;T) |
Make rs1363364(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 34817436 |
Gene | LINC01801 |
is a | snp |
is | mentioned by |
dbSNP | rs1363364 |
dbSNP (classic) | rs1363364 |
ClinGen | rs1363364 |
ebi | rs1363364 |
HLI | rs1363364 |
Exac | rs1363364 |
Gnomad | rs1363364 |
Varsome | rs1363364 |
LitVar | rs1363364 |
Map | rs1363364 |
PheGenI | rs1363364 |
Biobank | rs1363364 |
1000 genomes | rs1363364 |
hgdp | rs1363364 |
ensembl | rs1363364 |
geneview | rs1363364 |
scholar | rs1363364 |
rs1363364 | |
pharmgkb | rs1363364 |
gwascentral | rs1363364 |
openSNP | rs1363364 |
23andMe | rs1363364 |
SNPshot | rs1363364 |
SNPdbe | rs1363364 |
MSV3d | rs1363364 |
GWAS Ctlg | rs1363364 |
GMAF | 0.4702 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 19185281] Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea.