Have questions? Visit https://www.reddit.com/r/SNPedia

rs397516806

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397516806(A;T)
Make rs397516806(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position112455968
GenePTPN11
is asnp
is mentioned by
dbSNPrs397516806
ebirs397516806
HLIrs397516806
Exacrs397516806
Varsomers397516806
Maprs397516806
PheGenIrs397516806
hapmaprs397516806
1000 genomesrs397516806
hgdprs397516806
ensemblrs397516806
gopubmedrs397516806
geneviewrs397516806
scholarrs397516806
googlers397516806
pharmgkbrs397516806
gwascentralrs397516806
openSNPrs397516806
23andMers397516806
23andMe allrs397516806
SNP Nexus

SNPshotrs397516806
SNPdbers397516806
MSV3drs397516806
GWAS Ctlgrs397516806
Max Magnitude0
ClinVar
Risk rs397516806(G,T;G,T)
Alt rs397516806(G,T;G,T)
Reference rs397516806(A;A)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene PTPN11
CLNDBN not provided not specified
Reversed 0
HGVS NC_000012.11:g.112893772A>G; NC_000012.11:g.112893772A>T
CLNSRC
CLNACC RCV000159048.1, RCV000037653.2,