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rs1990932

From SNPedia

Orientationplus
Stabilizedplus
Make rs1990932(A;A)
Make rs1990932(A;G)
Make rs1990932(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position45937042
GeneNOVA2
is asnp
is mentioned by
dbSNPrs1990932
ebirs1990932
HLIrs1990932
Exacrs1990932
Varsomers1990932
Maprs1990932
PheGenIrs1990932
hapmaprs1990932
1000 genomesrs1990932
hgdprs1990932
ensemblrs1990932
gopubmedrs1990932
geneviewrs1990932
scholarrs1990932
googlers1990932
pharmgkbrs1990932
gwascentralrs1990932
openSNPrs1990932
23andMers1990932
23andMe allrs1990932
SNP Nexus

SNPshotrs1990932
SNPdbers1990932
MSV3drs1990932
GWAS Ctlgrs1990932
GMAF0.4366
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 20133464] Identification of a Second Kindred with Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Narrows Localization to a <3.5 Megabase Pair Region on Chromosome 19q13.3