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rs140872693

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs140872693(C;C)
Make rs140872693(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position16025218
GenePROM1
is asnp
is mentioned by
dbSNPrs140872693
ebirs140872693
HLIrs140872693
Exacrs140872693
Varsomers140872693
Maprs140872693
PheGenIrs140872693
hapmaprs140872693
1000 genomesrs140872693
hgdprs140872693
ensemblrs140872693
gopubmedrs140872693
geneviewrs140872693
scholarrs140872693
googlers140872693
pharmgkbrs140872693
gwascentralrs140872693
openSNPrs140872693
23andMers140872693
23andMe allrs140872693
SNP Nexus

SNPshotrs140872693
SNPdbers140872693
MSV3drs140872693
GWAS Ctlgrs140872693
Max Magnitude0
ClinVar
Risk rs140872693(C;C)
Alt rs140872693(C;C)
Reference rs140872693(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PROM1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.16026841G>C
CLNSRC
CLNACC RCV000171375.1,