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rs376239580

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs376239580(A;A)
Make rs376239580(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome20
Position5302632
GenePROKR2
is asnp
is mentioned by
dbSNPrs376239580
ebirs376239580
HLIrs376239580
Exacrs376239580
Varsomers376239580
Maprs376239580
PheGenIrs376239580
hapmaprs376239580
1000 genomesrs376239580
hgdprs376239580
ensemblrs376239580
gopubmedrs376239580
geneviewrs376239580
scholarrs376239580
googlers376239580
pharmgkbrs376239580
gwascentralrs376239580
openSNPrs376239580
23andMers376239580
23andMe allrs376239580
SNP Nexus

SNPshotrs376239580
SNPdbers376239580
MSV3drs376239580
GWAS Ctlgrs376239580
Max Magnitude0
ClinVar
Risk rs376239580(A;A)
Alt rs376239580(A;A)
Reference rs376239580(G;G)
Significance Probable-Pathogenic
Disease Hypogonadotrophic hypogonadism
Variation info
Gene PROKR2
CLNDBN Hypogonadotrophic hypogonadism
Reversed 0
HGVS NC_000020.10:g.5283278G>A
CLNSRC
CLNACC RCV000156965.1,