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rs267607034

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267607034(G;G)
Make rs267607034(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156163009
GeneSEMA4A
is asnp
is mentioned by
dbSNPrs267607034
ebirs267607034
HLIrs267607034
Exacrs267607034
Varsomers267607034
Maprs267607034
PheGenIrs267607034
hapmaprs267607034
1000 genomesrs267607034
hgdprs267607034
ensemblrs267607034
gopubmedrs267607034
geneviewrs267607034
scholarrs267607034
googlers267607034
pharmgkbrs267607034
gwascentralrs267607034
openSNPrs267607034
23andMers267607034
23andMe allrs267607034
SNP Nexus

SNPshotrs267607034
SNPdbers267607034
MSV3drs267607034
GWAS Ctlgrs267607034
Max Magnitude0
ClinVar
Risk rs267607034(G;G)
Alt rs267607034(G;G)
Reference rs267607034(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 35 Cone-rod dystrophy 10
Variation info
Gene SEMA4A
CLNDBN Retinitis pigmentosa 35 Cone-rod dystrophy 10
Reversed 0
HGVS NC_000001.10:g.156132800T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003526.3, RCV000003527.3,