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rs730880994

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880994(A;G)
Make rs730880994(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position112489036
GenePTPN11
is asnp
is mentioned by
dbSNPrs730880994
ebirs730880994
HLIrs730880994
Exacrs730880994
Varsomers730880994
Maprs730880994
PheGenIrs730880994
hapmaprs730880994
1000 genomesrs730880994
hgdprs730880994
ensemblrs730880994
gopubmedrs730880994
geneviewrs730880994
scholarrs730880994
googlers730880994
pharmgkbrs730880994
gwascentralrs730880994
openSNPrs730880994
23andMers730880994
23andMe allrs730880994
SNP Nexus

SNPshotrs730880994
SNPdbers730880994
MSV3drs730880994
GWAS Ctlgrs730880994
Max Magnitude0
ClinVar
Risk rs730880994(G;G)
Alt rs730880994(G;G)
Reference rs730880994(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112926840A>G
CLNSRC
CLNACC RCV000159055.2,