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rs869320772

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869320772(C;T)
Make rs869320772(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position515999
GenePIGG
is asnp
is mentioned by
dbSNPrs869320772
ebirs869320772
HLIrs869320772
Exacrs869320772
Varsomers869320772
Maprs869320772
PheGenIrs869320772
hapmaprs869320772
1000 genomesrs869320772
hgdprs869320772
ensemblrs869320772
gopubmedrs869320772
geneviewrs869320772
scholarrs869320772
googlers869320772
pharmgkbrs869320772
gwascentralrs869320772
openSNPrs869320772
23andMers869320772
23andMe allrs869320772
SNP Nexus

SNPshotrs869320772
SNPdbers869320772
MSV3drs869320772
GWAS Ctlgrs869320772
Max Magnitude0
ClinVar
Risk rs869320772(T;T)
Alt rs869320772(T;T)
Reference rs869320772(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene PIGG
CLNDBN Mental retardation, autosomal recessive 53
Reversed 0
HGVS NC_000004.11:g.509788C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000210943.1,