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rs555895

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs555895(G;G)
Make rs555895(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87961150
GenePTEN
is asnp
is mentioned by
dbSNPrs555895
ebirs555895
HLIrs555895
Exacrs555895
Varsomers555895
Maprs555895
PheGenIrs555895
hapmaprs555895
1000 genomesrs555895
hgdprs555895
ensemblrs555895
gopubmedrs555895
geneviewrs555895
scholarrs555895
googlers555895
pharmgkbrs555895
gwascentralrs555895
openSNPrs555895
23andMers555895
23andMe allrs555895
SNP Nexus

SNPshotrs555895
SNPdbers555895
MSV3drs555895
GWAS Ctlgrs555895
GMAF0.4339
Max Magnitude0

[PMID 23068025] Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese population [PMID 17033968OA-icon.png] Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.


[PMID 18805939OA-icon.png] Functional genetic polymorphisms and female reproductive disorders: part II--endometriosis.

ClinVar
Risk rs555895(G;G)
Alt rs555895(G;G)
Reference rs555895(T;T)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PTEN
CLNDBN not specified
Reversed 0
HGVS NC_000010.10:g.89720907T>G
CLNSRC ClinVar
CLNACC RCV000078603.3,



[PMID 26541596] Association of genetic polymorphisms in PTEN and additional gene-gene interaction with risk of esophageal squamous cell carcinoma in Chinese Han population