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rs587777864

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777864(A;A)
Make rs587777864(A;G)
ReferenceGRCh38 38.1/142
Chromosome3
Position71781588
GenePROK2
is asnp
is mentioned by
dbSNPrs587777864
ebirs587777864
HLIrs587777864
Exacrs587777864
Varsomers587777864
Maprs587777864
PheGenIrs587777864
hapmaprs587777864
1000 genomesrs587777864
hgdprs587777864
ensemblrs587777864
gopubmedrs587777864
geneviewrs587777864
scholarrs587777864
googlers587777864
pharmgkbrs587777864
gwascentralrs587777864
openSNPrs587777864
23andMers587777864
23andMe allrs587777864
SNP Nexus

SNPshotrs587777864
SNPdbers587777864
MSV3drs587777864
GWAS Ctlgrs587777864
Max Magnitude0
ClinVar
Risk rs587777864(A;A)
Alt rs587777864(A;A)
Reference rs587777864(G;G)
Significance Pathogenic
Disease Kallmann syndrome 4
Variation info
Gene PROK2
CLNDBN Kallmann syndrome 4
Reversed 1
HGVS NC_000003.11:g.71830739C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144711.3,