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rs1057517850

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517850(C;T)
Make rs1057517850(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position112477974
GenePTPN11
is asnp
is mentioned by
dbSNPrs1057517850
dbSNP (old)rs1057517850
ClinGenrs1057517850
ebirs1057517850
HLIrs1057517850
Exacrs1057517850
Gnomadrs1057517850
Varsomers1057517850
Maprs1057517850
PheGenIrs1057517850
Biobankrs1057517850
1000 genomesrs1057517850
hgdprs1057517850
ensemblrs1057517850
gopubmedrs1057517850
geneviewrs1057517850
scholarrs1057517850
googlers1057517850
pharmgkbrs1057517850
gwascentralrs1057517850
openSNPrs1057517850
23andMers1057517850
23andMe allrs1057517850
SNPshotrs1057517850
SNPdbers1057517850
MSV3drs1057517850
GWAS Ctlgrs1057517850
Max Magnitude0
ClinVar
Risk rs1057517850(T;T)
Alt rs1057517850(T;T)
Reference Rs1057517850(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PTPN11
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.112915778C>T
CLNSRC
CLNACC RCV000413347.1,