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rs1057520208

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 6.3 Hereditary cancer predisposing syndrome
(G;G) 0 common/normal


Make rs1057520208(A;A)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position87933012
GenePTEN
is asnp
is mentioned by
dbSNPrs1057520208
dbSNP (old)rs1057520208
ClinGenrs1057520208
ebirs1057520208
HLIrs1057520208
Exacrs1057520208
Gnomadrs1057520208
Varsomers1057520208
Maprs1057520208
PheGenIrs1057520208
Biobankrs1057520208
1000 genomesrs1057520208
hgdprs1057520208
ensemblrs1057520208
gopubmedrs1057520208
geneviewrs1057520208
scholarrs1057520208
googlers1057520208
pharmgkbrs1057520208
gwascentralrs1057520208
openSNPrs1057520208
23andMers1057520208
23andMe allrs1057520208
SNPshotrs1057520208
SNPdbers1057520208
MSV3drs1057520208
GWAS Ctlgrs1057520208
Max Magnitude6.3
ClinVar
Risk rs1057520208(A;A)
Alt rs1057520208(A;A)
Reference Rs1057520208(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PTEN
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.89692769G>A
CLNSRC
CLNACC RCV000434799.1,