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rs10922153

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs10922153(G;G)
Make rs10922153(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position197009485
GeneCFHR5
is asnp
is mentioned by
dbSNPrs10922153
dbSNP (classic)rs10922153
ClinGenrs10922153
ebirs10922153
HLIrs10922153
Exacrs10922153
Gnomadrs10922153
Varsomers10922153
LitVarrs10922153
Maprs10922153
PheGenIrs10922153
Biobankrs10922153
1000 genomesrs10922153
hgdprs10922153
ensemblrs10922153
geneviewrs10922153
scholarrs10922153
googlers10922153
pharmgkbrs10922153
gwascentralrs10922153
openSNPrs10922153
23andMers10922153
SNPshotrs10922153
SNPdbers10922153
MSV3drs10922153
GWAS Ctlgrs10922153
GMAF0.3173
Max Magnitude0
? (G;G) (G;T) (T;T) 28


[PMID 23582991] Genetic Influences on the Outcome of Anti-Vascular Endothelial Growth Factor Treatment in Neovascular Age-related Macular Degeneration


[PMID 18541031OA-icon.png] The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.


[PMID 19801603OA-icon.png] Rapid inexpensive genome-wide association using pooled whole blood.


ClinVar
Risk rs10922153(G;G)
Alt rs10922153(G;G)
Reference Rs10922153(T;T)
Significance Non-pathogenic
Disease Mesangiocapillary glomerulonephritis
Variation info
Gene CFHR5
CLNDBN Mesangiocapillary glomerulonephritis, type II
Reversed 0
HGVS NC_000001.10:g.196978615T>G
CLNSRC
CLNACC RCV000294081.1,