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rs864622451

From SNPedia

Orientationplus
Make rs864622451(-;-)
Make rs864622451(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position87960937
GenePTEN
is asnp
is mentioned by
dbSNPrs864622451
ebirs864622451
HLIrs864622451
Exacrs864622451
Varsomers864622451
Maprs864622451
PheGenIrs864622451
hapmaprs864622451
1000 genomesrs864622451
hgdprs864622451
ensemblrs864622451
gopubmedrs864622451
geneviewrs864622451
scholarrs864622451
googlers864622451
pharmgkbrs864622451
gwascentralrs864622451
openSNPrs864622451
23andMers864622451
23andMe allrs864622451
SNP Nexus

SNPshotrs864622451
SNPdbers864622451
MSV3drs864622451
GWAS Ctlgrs864622451
Max Magnitude
ClinVar
Risk rs864622451(;)
Alt rs864622451(;)
Reference rs864622451(G;G)
Significance Pathogenic
Disease PTEN hamartoma tumor syndrome
Variation info
Gene PTEN
CLNDBN PTEN hamartoma tumor syndrome
Reversed 0
HGVS NC_000010.10:g.89720694delG
CLNSRC
CLNACC RCV000204863.1,