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rs786204881

From SNPedia

Orientationplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs786204881(-;-)
Make rs786204881(-;GA)
Make rs786204881(GA;GA)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87864490
GeneKLLN, PTEN
is asnp
is mentioned by
dbSNPrs786204881
ebirs786204881
HLIrs786204881
Exacrs786204881
Varsomers786204881
Maprs786204881
PheGenIrs786204881
hapmaprs786204881
1000 genomesrs786204881
hgdprs786204881
ensemblrs786204881
gopubmedrs786204881
geneviewrs786204881
scholarrs786204881
googlers786204881
pharmgkbrs786204881
gwascentralrs786204881
openSNPrs786204881
23andMers786204881
23andMe allrs786204881
SNP Nexus

SNPshotrs786204881
SNPdbers786204881
MSV3drs786204881
GWAS Ctlgrs786204881
Max Magnitude0
ClinVar
Risk rs786204881(;)
Alt rs786204881(;)
Reference rs786204881(AG;AG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene PTEN LOC101929706 KLLN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000010.10:g.89624247_89624248delGA
CLNSRC
CLNACC RCV000169822.1,