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rs398122522

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398122522(A;G)
Make rs398122522(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position35070174
GenePRLR
is asnp
is mentioned by
dbSNPrs398122522
ebirs398122522
HLIrs398122522
Exacrs398122522
Varsomers398122522
Maprs398122522
PheGenIrs398122522
hapmaprs398122522
1000 genomesrs398122522
hgdprs398122522
ensemblrs398122522
gopubmedrs398122522
geneviewrs398122522
scholarrs398122522
googlers398122522
pharmgkbrs398122522
gwascentralrs398122522
openSNPrs398122522
23andMers398122522
23andMe allrs398122522
SNP Nexus

SNPshotrs398122522
SNPdbers398122522
MSV3drs398122522
GWAS Ctlgrs398122522
Max Magnitude0
ClinVar
Risk rs398122522(G;G)
Alt rs398122522(G;G)
Reference rs398122522(A;A)
Significance Pathogenic
Disease Hyperprolactinemia
Variation info
Gene PRLR
CLNDBN Hyperprolactinemia
Reversed 1
HGVS NC_000005.9:g.35070276T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000074500.12,