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rs434102

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs434102(C;C)
Make rs434102(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position42698323
GenePRPH2
is asnp
is mentioned by
dbSNPrs434102
ebirs434102
HLIrs434102
Exacrs434102
Varsomers434102
Maprs434102
PheGenIrs434102
hapmaprs434102
1000 genomesrs434102
hgdprs434102
ensemblrs434102
gopubmedrs434102
geneviewrs434102
scholarrs434102
googlers434102
pharmgkbrs434102
gwascentralrs434102
openSNPrs434102
23andMers434102
23andMe allrs434102
SNP Nexus

SNPshotrs434102
SNPdbers434102
MSV3drs434102
GWAS Ctlgrs434102
GMAF0.219
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 22948568] Evaluation of the ELOVL4, PRPH2 and ABCA4 genes in patients with Stargardt macular degeneration


ClinVar
Risk rs434102(C;C)
Alt rs434102(C;C)
Reference rs434102(T;T)
Significance Probable-non-pathogenic
Disease not provided not specified
Variation info
Gene PRPH2
CLNDBN not provided not specified
Reversed 0
HGVS NC_000006.11:g.42666061T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000127756.4, RCV000153779.3,



[PMID 26849151] Evaluation of the association of single nucleotide polymorphisms in the PRPH2 gene with adult-onset foveomacular vitelliform dystrophy.