rs16982345
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16982345(A;A) |
Make rs16982345(A;G) |
Make rs16982345(G;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 19 |
Position | 18389912 |
is a | snp |
is | mentioned by |
dbSNP | rs16982345 |
dbSNP (classic) | rs16982345 |
ClinGen | rs16982345 |
ebi | rs16982345 |
HLI | rs16982345 |
Exac | rs16982345 |
Gnomad | rs16982345 |
Varsome | rs16982345 |
LitVar | rs16982345 |
Map | rs16982345 |
PheGenI | rs16982345 |
Biobank | rs16982345 |
1000 genomes | rs16982345 |
hgdp | rs16982345 |
ensembl | rs16982345 |
geneview | rs16982345 |
scholar | rs16982345 |
rs16982345 | |
pharmgkb | rs16982345 |
gwascentral | rs16982345 |
openSNP | rs16982345 |
23andMe | rs16982345 |
SNPshot | rs16982345 |
SNPdbe | rs16982345 |
MSV3d | rs16982345 |
GWAS Ctlg | rs16982345 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Reported in [PMID 29563502] as influencing hyperemesis gravidarum (more commonly known as pregnancy-associated morning sickness).
Note that although the rs16982345(G) allele is reported as increasing risk (by ~1.5x) for morning sickness, since ~75% of all alleles are the (G) allele, it might be more helpful to think of the (A) allele as being slightly protective.