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rs36212732

From SNPedia

Orientationplus
Stabilizedplus
Make rs36212732(A;A)
Make rs36212732(A;G)
Make rs36212732(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position122455682
GeneARMS2, LOC105378525
is asnp
is mentioned by
dbSNPrs36212732
dbSNP (classic)rs36212732
ClinGenrs36212732
ebirs36212732
HLIrs36212732
Exacrs36212732
Gnomadrs36212732
Varsomers36212732
LitVarrs36212732
Maprs36212732
PheGenIrs36212732
Biobankrs36212732
1000 genomesrs36212732
hgdprs36212732
ensemblrs36212732
geneviewrs36212732
scholarrs36212732
googlers36212732
pharmgkbrs36212732
gwascentralrs36212732
openSNPrs36212732
23andMers36212732
SNPshotrs36212732
SNPdbers36212732
MSV3drs36212732
GWAS Ctlgrs36212732
Max Magnitude0

[PMID 28659708OA-icon.png] Specific correlation between the major chromosome 10q26 haplotype conferring risk for age-related macular degeneration and the expression of HTRA1.