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rs746174328

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs746174328(-;-)
Make rs746174328(-;TA)
Make rs746174328(TA;TA)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position16009072
GenePROM1
is asnp
is mentioned by
dbSNPrs746174328
ebirs746174328
HLIrs746174328
Exacrs746174328
Varsomers746174328
Maprs746174328
PheGenIrs746174328
hapmaprs746174328
1000 genomesrs746174328
hgdprs746174328
ensemblrs746174328
gopubmedrs746174328
geneviewrs746174328
scholarrs746174328
googlers746174328
pharmgkbrs746174328
gwascentralrs746174328
openSNPrs746174328
23andMers746174328
23andMe allrs746174328
SNP Nexus

SNPshotrs746174328
SNPdbers746174328
MSV3drs746174328
GWAS Ctlgrs746174328
Max Magnitude0
ClinVar
Risk rs746174328(;)
Alt rs746174328(;)
Reference rs746174328(AT;AT)
Significance Pathogenic
Disease Retinitis pigmentosa 41
Variation info
Gene PROM1
CLNDBN Retinitis pigmentosa 41
Reversed 0
HGVS NC_000004.11:g.16010695_16010696delAT
CLNSRC
CLNACC RCV000190617.1,