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rs587777863

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777863(C;C)
Make rs587777863(C;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position71784983
GenePROK2
is asnp
is mentioned by
dbSNPrs587777863
ebirs587777863
HLIrs587777863
Exacrs587777863
Varsomers587777863
Maprs587777863
PheGenIrs587777863
hapmaprs587777863
1000 genomesrs587777863
hgdprs587777863
ensemblrs587777863
gopubmedrs587777863
geneviewrs587777863
scholarrs587777863
googlers587777863
pharmgkbrs587777863
gwascentralrs587777863
openSNPrs587777863
23andMers587777863
23andMe allrs587777863
SNP Nexus

SNPshotrs587777863
SNPdbers587777863
MSV3drs587777863
GWAS Ctlgrs587777863
Max Magnitude0
ClinVar
Risk rs587777863(C;C)
Alt rs587777863(C;C)
Reference rs587777863(G;G)
Significance Pathogenic
Disease Kallmann syndrome 4
Variation info
Gene PROK2
CLNDBN Kallmann syndrome 4
Reversed 1
HGVS NC_000003.11:g.71834134C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000144710.3,