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rs553443857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs553443857(G;T)
Make rs553443857(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2135425
GeneIGF2, INS-IGF2, MIR483
is asnp
is mentioned by
dbSNPrs553443857
dbSNP (classic)rs553443857
ClinGenrs553443857
ebirs553443857
HLIrs553443857
Exacrs553443857
Gnomadrs553443857
Varsomers553443857
LitVarrs553443857
Maprs553443857
PheGenIrs553443857
Biobankrs553443857
1000 genomesrs553443857
hgdprs553443857
ensemblrs553443857
geneviewrs553443857
scholarrs553443857
googlers553443857
pharmgkbrs553443857
gwascentralrs553443857
openSNPrs553443857
23andMers553443857
SNPshotrs553443857
SNPdbers553443857
MSV3drs553443857
GWAS Ctlgrs553443857
Max Magnitude0
ClinVar
Risk rs553443857(A;A) rs553443857(T;T)
Alt rs553443857(A;A) rs553443857(T;T)
Reference Rs553443857(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MIR483 IGF2 INS-IGF2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.2156655G>T
CLNSRC
CLNACC RCV000412860.1,