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rs71455367

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs71455367(C;C)
Make rs71455367(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position11268104
GenePRB3
is asnp
is mentioned by
dbSNPrs71455367
ebirs71455367
HLIrs71455367
Exacrs71455367
Varsomers71455367
Maprs71455367
PheGenIrs71455367
hapmaprs71455367
1000 genomesrs71455367
hgdprs71455367
ensemblrs71455367
gopubmedrs71455367
geneviewrs71455367
scholarrs71455367
googlers71455367
pharmgkbrs71455367
gwascentralrs71455367
openSNPrs71455367
23andMers71455367
23andMe allrs71455367
SNP Nexus

SNPshotrs71455367
SNPdbers71455367
MSV3drs71455367
GWAS Ctlgrs71455367
Max Magnitude0
OMIM168840
Desc
Variant0001
Relatedalso
ClinVar
Risk rs71455367(A,C;A,C)
Alt rs71455367(A,C;A,C)
Reference rs71455367(G;G)
Significance Pathogenic
Disease PRB3S(CYS)
Variation info
Gene PRB3
CLNDBN PRB3S(CYS)
Reversed 0
HGVS NC_000012.11:g.11421038G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014736.25,