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rs779886453

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs779886453(-;-)
Make rs779886453(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position29073315
GeneC2orf71, LOC105374385
is asnp
is mentioned by
dbSNPrs779886453
ebirs779886453
HLIrs779886453
Exacrs779886453
Varsomers779886453
Maprs779886453
PheGenIrs779886453
hapmaprs779886453
1000 genomesrs779886453
hgdprs779886453
ensemblrs779886453
gopubmedrs779886453
geneviewrs779886453
scholarrs779886453
googlers779886453
pharmgkbrs779886453
gwascentralrs779886453
openSNPrs779886453
23andMers779886453
23andMe allrs779886453
SNP Nexus

SNPshotrs779886453
SNPdbers779886453
MSV3drs779886453
GWAS Ctlgrs779886453
Max Magnitude0
ClinVar
Risk rs779886453(;)
Alt rs779886453(;)
Reference rs779886453(T;T)
Significance Pathogenic
Disease Retinitis pigmentosa 54
Variation info
Gene C2orf71
CLNDBN Retinitis pigmentosa 54
Reversed 0
HGVS NC_000002.11:g.29296181delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000000123.3,