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rs1057524907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524907(A;G)
Make rs1057524907(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position2159907
GeneINS, INS-IGF2
is asnp
is mentioned by
dbSNPrs1057524907
dbSNP (old)rs1057524907
ClinGenrs1057524907
ebirs1057524907
HLIrs1057524907
Exacrs1057524907
Gnomadrs1057524907
Varsomers1057524907
LitVarrs1057524907
Maprs1057524907
PheGenIrs1057524907
Biobankrs1057524907
1000 genomesrs1057524907
hgdprs1057524907
ensemblrs1057524907
gopubmedrs1057524907
geneviewrs1057524907
scholarrs1057524907
googlers1057524907
pharmgkbrs1057524907
gwascentralrs1057524907
openSNPrs1057524907
23andMers1057524907
23andMe allrs1057524907
SNPshotrs1057524907
SNPdbers1057524907
MSV3drs1057524907
GWAS Ctlgrs1057524907
Max Magnitude0
ClinVar
Risk rs1057524907(G;G)
Alt rs1057524907(G;G)
Reference Rs1057524907(A;A)
Significance Probable-Pathogenic
Disease Monogenic diabetes
Variation info
Gene INS INS-IGF2
CLNDBN Monogenic diabetes
Reversed 1
HGVS NC_000011.9:g.2181137T>C
CLNSRC
CLNACC RCV000445381.1,