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rs727504107

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504107(C;T)
Make rs727504107(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
GenePRPF31
is asnp
is mentioned by
dbSNPrs727504107
ebirs727504107
HLIrs727504107
Exacrs727504107
Varsomers727504107
Maprs727504107
PheGenIrs727504107
hapmaprs727504107
1000 genomesrs727504107
hgdprs727504107
ensemblrs727504107
gopubmedrs727504107
geneviewrs727504107
scholarrs727504107
googlers727504107
pharmgkbrs727504107
gwascentralrs727504107
openSNPrs727504107
23andMers727504107
23andMe allrs727504107
SNP Nexus

SNPshotrs727504107
SNPdbers727504107
MSV3drs727504107
GWAS Ctlgrs727504107
Max Magnitude0
ClinVar
Risk rs727504107(T;T)
Alt rs727504107(T;T)
Reference rs727504107(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 11
Variation info
Gene PRPF31
CLNDBN Retinitis pigmentosa 11
Reversed 0
HGVS NC_000019.9:g.54632558C>T
CLNSRC
CLNACC RCV000153774.3,