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rs1136511

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1136511(A;A)
Make rs1136511(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position70033186
GeneHTN3
is asnp
is mentioned by
dbSNPrs1136511
ebirs1136511
HLIrs1136511
Exacrs1136511
Varsomers1136511
Maprs1136511
PheGenIrs1136511
hapmaprs1136511
1000 genomesrs1136511
hgdprs1136511
ensemblrs1136511
gopubmedrs1136511
geneviewrs1136511
scholarrs1136511
googlers1136511
pharmgkbrs1136511
gwascentralrs1136511
openSNPrs1136511
23andMers1136511
23andMe allrs1136511
SNP Nexus

SNPshotrs1136511
SNPdbers1136511
MSV3drs1136511
GWAS Ctlgrs1136511
Max Magnitude0
ClinVar
Risk rs1136511(A;A)
Alt rs1136511(A;A)
Reference rs1136511(G;G)
Significance Pathogenic
Disease HIS2*1/HIS2*2 POLYMORPHISM
Variation info
Gene HTN3
CLNDBN HIS2*1/HIS2*2 POLYMORPHISM
Reversed 0
HGVS NC_000004.11:g.70898903G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016048.2,