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rs587777834

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777834(-;-)
Make rs587777834(-;C)
ReferenceGRCh38 38.1/142
Chromosome20
Position5314312
GeneFLJ33544, PROKR2
is asnp
is mentioned by
dbSNPrs587777834
ebirs587777834
HLIrs587777834
Exacrs587777834
Varsomers587777834
Maprs587777834
PheGenIrs587777834
hapmaprs587777834
1000 genomesrs587777834
hgdprs587777834
ensemblrs587777834
gopubmedrs587777834
geneviewrs587777834
scholarrs587777834
googlers587777834
pharmgkbrs587777834
gwascentralrs587777834
openSNPrs587777834
23andMers587777834
23andMe allrs587777834
SNP Nexus

SNPshotrs587777834
SNPdbers587777834
MSV3drs587777834
GWAS Ctlgrs587777834
Max Magnitude0
ClinVar
Risk rs587777834(;)
Alt rs587777834(;)
Reference rs587777834(C;C)
Significance Pathogenic
Disease Kallmann syndrome 3
Variation info
Gene LOC728283 PROKR2
CLNDBN Kallmann syndrome 3
Reversed 1
HGVS NC_000020.10:g.5294958delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000022409.5,