Have questions? Visit https://www.reddit.com/r/SNPedia

rs577932201

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs577932201(C;T)
Make rs577932201(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position21325330
GeneRPGRIP1
is asnp
is mentioned by
dbSNPrs577932201
ebirs577932201
HLIrs577932201
Exacrs577932201
Varsomers577932201
Maprs577932201
PheGenIrs577932201
hapmaprs577932201
1000 genomesrs577932201
hgdprs577932201
ensemblrs577932201
gopubmedrs577932201
geneviewrs577932201
scholarrs577932201
googlers577932201
pharmgkbrs577932201
gwascentralrs577932201
openSNPrs577932201
23andMers577932201
23andMe allrs577932201
SNP Nexus

SNPshotrs577932201
SNPdbers577932201
MSV3drs577932201
GWAS Ctlgrs577932201
Max Magnitude0
ClinVar
Risk rs577932201(T;T)
Alt rs577932201(T;T)
Reference rs577932201(C;C)
Significance Probable-Pathogenic
Disease Retinal dystrophy
Variation info
Gene RPGRIP1
CLNDBN Retinal dystrophy
Reversed 0
HGVS NC_000014.8:g.21793489C>T
CLNSRC
CLNACC RCV000225680.1,