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rs387907116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387907116(A;A)
Make rs387907116(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position232263247
GeneDIS3L2
is asnp
is mentioned by
dbSNPrs387907116
ebirs387907116
HLIrs387907116
Exacrs387907116
Varsomers387907116
Maprs387907116
PheGenIrs387907116
hapmaprs387907116
1000 genomesrs387907116
hgdprs387907116
ensemblrs387907116
gopubmedrs387907116
geneviewrs387907116
scholarrs387907116
googlers387907116
pharmgkbrs387907116
gwascentralrs387907116
openSNPrs387907116
23andMers387907116
23andMe allrs387907116
SNP Nexus

SNPshotrs387907116
SNPdbers387907116
MSV3drs387907116
GWAS Ctlgrs387907116
Max Magnitude0
ClinVar
Risk rs387907116(A;A)
Alt rs387907116(A;A)
Reference rs387907116(G;G)
Significance Pathogenic
Disease Renal hamartomas nephroblastomatosis and fetal gigantism
Variation info
Gene DIS3L2
CLNDBN Renal hamartomas nephroblastomatosis and fetal gigantism
Reversed 0
HGVS NC_000002.11:g.233127957G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000024121.3,