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rs16982345

From SNPedia

Orientationplus
Stabilizedplus
Make rs16982345(A;A)
Make rs16982345(A;G)
Make rs16982345(G;G)
ReferenceGRCh38.p7 38.3/151
Chromosome19
Position18389912
is asnp
is mentioned by
dbSNPrs16982345
dbSNP (classic)rs16982345
ClinGenrs16982345
ebirs16982345
HLIrs16982345
Exacrs16982345
Gnomadrs16982345
Varsomers16982345
LitVarrs16982345
Maprs16982345
PheGenIrs16982345
Biobankrs16982345
1000 genomesrs16982345
hgdprs16982345
ensemblrs16982345
geneviewrs16982345
scholarrs16982345
googlers16982345
pharmgkbrs16982345
gwascentralrs16982345
openSNPrs16982345
23andMers16982345
SNPshotrs16982345
SNPdbers16982345
MSV3drs16982345
GWAS Ctlgrs16982345
Max Magnitude0
? (A;A) (A;G) (G;G) 28


Reported in [PMID 29563502OA-icon.png] 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.