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rs869320773

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869320773(C;C)
Make rs869320773(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position527231
GenePIGG
is asnp
is mentioned by
dbSNPrs869320773
ebirs869320773
HLIrs869320773
Exacrs869320773
Varsomers869320773
Maprs869320773
PheGenIrs869320773
hapmaprs869320773
1000 genomesrs869320773
hgdprs869320773
ensemblrs869320773
gopubmedrs869320773
geneviewrs869320773
scholarrs869320773
googlers869320773
pharmgkbrs869320773
gwascentralrs869320773
openSNPrs869320773
23andMers869320773
23andMe allrs869320773
SNP Nexus

SNPshotrs869320773
SNPdbers869320773
MSV3drs869320773
GWAS Ctlgrs869320773
Max Magnitude0
ClinVar
Risk rs869320773(C;C)
Alt rs869320773(C;C)
Reference rs869320773(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene PIGG
CLNDBN Mental retardation, autosomal recessive 53
Reversed 0
HGVS NC_000004.11:g.521020G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000210941.1,