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rs10895322

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10895322(A;G)
Make rs10895322(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position102599525
GeneMMP20
is asnp
is mentioned by
dbSNPrs10895322
ebirs10895322
HLIrs10895322
Exacrs10895322
Varsomers10895322
Maprs10895322
PheGenIrs10895322
hapmaprs10895322
1000 genomesrs10895322
hgdprs10895322
ensemblrs10895322
gopubmedrs10895322
geneviewrs10895322
scholarrs10895322
googlers10895322
pharmgkbrs10895322
gwascentralrs10895322
openSNPrs10895322
23andMers10895322
23andMe allrs10895322
SNP Nexus

SNPshotrs10895322
SNPdbers10895322
MSV3drs10895322
GWAS Ctlgrs10895322
Max Magnitude0
? (A;A) (A;G) (G;G) 28

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

ClinVar
Risk rs10895322(G;G)
Alt rs10895322(G;G)
Reference rs10895322(A;A)
Significance Untested
Disease not provided
Variation info
Gene MMP20
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.102470256A>G
CLNSRC
CLNACC RCV000190296.1,