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rs5030774

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs5030774(A;A)
Make rs5030774(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position49016130
GeneLHB, RUVBL2
is asnp
is mentioned by
dbSNPrs5030774
ebirs5030774
HLIrs5030774
Exacrs5030774
Varsomers5030774
Maprs5030774
PheGenIrs5030774
hapmaprs5030774
1000 genomesrs5030774
hgdprs5030774
ensemblrs5030774
gopubmedrs5030774
geneviewrs5030774
scholarrs5030774
googlers5030774
pharmgkbrs5030774
gwascentralrs5030774
openSNPrs5030774
23andMers5030774
23andMe allrs5030774
SNP Nexus

SNPshotrs5030774
SNPdbers5030774
MSV3drs5030774
GWAS Ctlgrs5030774
GMAF0.0009183
Max Magnitude0
OMIM152780
Desc
Variant0003
Relatedalso
ClinVar
Risk rs5030774(A;A)
Alt rs5030774(A;A)
Reference rs5030774(G;G)
Significance Pathogenic
Disease Infertility
Variation info
Gene RUVBL2 LHB
CLNDBN Infertility, male and female
Reversed 1
HGVS NC_000019.9:g.49519387C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015496.29,