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rs111784356

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs111784356(A;A)
Make rs111784356(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position101229574
GeneIMPG2
is asnp
is mentioned by
dbSNPrs111784356
ebirs111784356
HLIrs111784356
Exacrs111784356
Varsomers111784356
Maprs111784356
PheGenIrs111784356
hapmaprs111784356
1000 genomesrs111784356
hgdprs111784356
ensemblrs111784356
gopubmedrs111784356
geneviewrs111784356
scholarrs111784356
googlers111784356
pharmgkbrs111784356
gwascentralrs111784356
openSNPrs111784356
23andMers111784356
23andMe allrs111784356
SNP Nexus

SNPshotrs111784356
SNPdbers111784356
MSV3drs111784356
GWAS Ctlgrs111784356
Max Magnitude0
ClinVar
Risk rs111784356(A;A)
Alt rs111784356(A;A)
Reference rs111784356(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IMPG2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.100948418G>A
CLNSRC
CLNACC RCV000171365.1,