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rs1120638

From SNPedia

Orientationminus
Stabilizedminus
Make rs1120638(A;A)
Make rs1120638(A;G)
Make rs1120638(G;G)
ReferenceGRCh37.p2 37.2/134
ChromosomeX
Position89247084
is asnp
is mentioned by
dbSNPrs1120638
ebirs1120638
HLIrs1120638
Exacrs1120638
Varsomers1120638
Maprs1120638
PheGenIrs1120638
hapmaprs1120638
1000 genomesrs1120638
hgdprs1120638
ensemblrs1120638
gopubmedrs1120638
geneviewrs1120638
scholarrs1120638
googlers1120638
pharmgkbrs1120638
gwascentralrs1120638
openSNPrs1120638
23andMers1120638
23andMe allrs1120638
SNP Nexus

SNPshotrs1120638
SNPdbers1120638
MSV3drs1120638
GWAS Ctlgrs1120638
Max Magnitude

[PMID 21882634] [Influence of genetic mutations on clinical presentation of subretinal neovascularization. Report 2: The impact of HTRA and VEGF genes polymorphism][PMID 18493315OA-icon.png] C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes.