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rs267607033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607033(C;C)
Make rs267607033(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156162993
GeneSEMA4A
is asnp
is mentioned by
dbSNPrs267607033
ebirs267607033
HLIrs267607033
Exacrs267607033
Varsomers267607033
Maprs267607033
PheGenIrs267607033
hapmaprs267607033
1000 genomesrs267607033
hgdprs267607033
ensemblrs267607033
gopubmedrs267607033
geneviewrs267607033
scholarrs267607033
googlers267607033
pharmgkbrs267607033
gwascentralrs267607033
openSNPrs267607033
23andMers267607033
23andMe allrs267607033
SNP Nexus

SNPshotrs267607033
SNPdbers267607033
MSV3drs267607033
GWAS Ctlgrs267607033
Max Magnitude0
ClinVar
Risk rs267607033(C;C)
Alt rs267607033(C;C)
Reference rs267607033(G;G)
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.156132784G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003524.3, RCV000003525.3,