Have questions? Visit https://www.reddit.com/r/SNPedia

rs2284665

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2284665(G;T)
Make rs2284665(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position122467114
GeneHTRA1
is asnp
is mentioned by
dbSNPrs2284665
dbSNP (classic)rs2284665
ClinGenrs2284665
ebirs2284665
HLIrs2284665
Exacrs2284665
Gnomadrs2284665
Varsomers2284665
LitVarrs2284665
Maprs2284665
PheGenIrs2284665
Biobankrs2284665
1000 genomesrs2284665
hgdprs2284665
ensemblrs2284665
geneviewrs2284665
scholarrs2284665
googlers2284665
pharmgkbrs2284665
gwascentralrs2284665
openSNPrs2284665
23andMers2284665
SNPshotrs2284665
SNPdbers2284665
MSV3drs2284665
GWAS Ctlgrs2284665
Max Magnitude0
? (G;G) (G;T) (T;T) 28


[PMID 26337002] MMP20 and ARMS2/HTRA1 Are Associated with Neovascular Lesion Size in Age-Related Macular Degeneration

ClinVar
Risk rs2284665(A;A) rs2284665(T;T)
Alt rs2284665(A;A) rs2284665(T;T)
Reference Rs2284665(G;G)
Significance Untested
Disease not provided
Variation info
Gene HTRA1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.124226630G>T
CLNSRC
CLNACC RCV000190309.1,