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

rs727503381

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727503381(A;T)
Make rs727503381(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position112454636
GenePTPN11
is asnp
is mentioned by
dbSNPrs727503381
ebirs727503381
HLIrs727503381
Exacrs727503381
Varsomers727503381
Maprs727503381
PheGenIrs727503381
hapmaprs727503381
1000 genomesrs727503381
hgdprs727503381
ensemblrs727503381
gopubmedrs727503381
geneviewrs727503381
scholarrs727503381
googlers727503381
pharmgkbrs727503381
gwascentralrs727503381
openSNPrs727503381
23andMers727503381
23andMe allrs727503381
SNP Nexus

SNPshotrs727503381
SNPdbers727503381
MSV3drs727503381
GWAS Ctlgrs727503381
Max Magnitude0
ClinVar
Risk rs727503381(T;T)
Alt rs727503381(T;T)
Reference rs727503381(A;A)
Significance Pathogenic
Disease Noonan syndrome
Variation info
Gene PTPN11
CLNDBN Noonan syndrome
Reversed 0
HGVS NC_000012.11:g.112892440A>T
CLNSRC
CLNACC RCV000151696.2,