Rs104894184

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Orientationplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs104894184(A;A)
Make rs104894184(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position87952159
GenePTEN
is asnp
is mentioned by
dbSNPrs104894184
Exacrs104894184
PheGenIrs104894184
nextbiors104894184
hapmaprs104894184
1000 genomesrs104894184
hgdprs104894184
ensemblrs104894184
gopubmedrs104894184
geneviewrs104894184
scholarrs104894184
googlers104894184
pharmgkbrs104894184
gwascentralrs104894184
openSNPrs104894184
23andMers104894184
23andMe allrs104894184
SNP Nexus

SNPshotrs104894184
SNPdbers104894184
MSV3drs104894184
Max Magnitude0
OMIM601728
Desc
Variant0014
Relatedalso
ClinVar
Risk rs104894184(A,G;A,G)
Alt rs104894184(A,G;A,G)
Reference rs104894184(T;T)
Significance Untested
Disease
Variation info
Gene PTEN
CLNDBN
Reversed 0
HGVS NC_000010.10:g.89711916T>A; NC_000010.10:g.89711916T>G
CLNSRC
CLNACC