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rs201247699

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201247699(C;C)
Make rs201247699(C;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position112486476
GenePTPN11
is asnp
is mentioned by
dbSNPrs201247699
ebirs201247699
HLIrs201247699
Exacrs201247699
Varsomers201247699
Maprs201247699
PheGenIrs201247699
hapmaprs201247699
1000 genomesrs201247699
hgdprs201247699
ensemblrs201247699
gopubmedrs201247699
geneviewrs201247699
scholarrs201247699
googlers201247699
pharmgkbrs201247699
gwascentralrs201247699
openSNPrs201247699
23andMers201247699
23andMe allrs201247699
SNP Nexus

SNPshotrs201247699
SNPdbers201247699
MSV3drs201247699
GWAS Ctlgrs201247699
Max Magnitude0
ClinVar
Risk rs201247699(C;C)
Alt rs201247699(C;C)
Reference rs201247699(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene PTPN11
CLNDBN not specified
Reversed 0
HGVS NC_000012.11:g.112924280G>C
CLNSRC ClinVar
CLNACC RCV000037608.3,