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rs1064795103

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position134417209
GenePHF6
is asnp
is mentioned by
dbSNPrs1064795103
dbSNP (classic)rs1064795103
ClinGenrs1064795103
ebirs1064795103
HLIrs1064795103
Exacrs1064795103
Gnomadrs1064795103
Varsomers1064795103
LitVarrs1064795103
Maprs1064795103
PheGenIrs1064795103
Biobankrs1064795103
1000 genomesrs1064795103
hgdprs1064795103
ensemblrs1064795103
geneviewrs1064795103
scholarrs1064795103
googlers1064795103
pharmgkbrs1064795103
gwascentralrs1064795103
openSNPrs1064795103
23andMers1064795103
23andMe allrs1064795103
SNPshotrs1064795103
SNPdbers1064795103
MSV3drs1064795103
GWAS Ctlgrs1064795103
Max Magnitude0
ClinVar
Risk rs1064795103(A;A)
Alt rs1064795103(A;A)
Reference Rs1064795103(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PHF6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.133551239G>A
CLNSRC
CLNACC RCV000481139.1,