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rs797044908

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs797044908(AA;AA)
Make rs797044908(AA;TG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position134417249
GenePHF6
is asnp
is mentioned by
dbSNPrs797044908
dbSNP (old)rs797044908
ClinGenrs797044908
ebirs797044908
HLIrs797044908
Exacrs797044908
Gnomadrs797044908
Varsomers797044908
Maprs797044908
PheGenIrs797044908
Biobankrs797044908
1000 genomesrs797044908
hgdprs797044908
ensemblrs797044908
gopubmedrs797044908
geneviewrs797044908
scholarrs797044908
googlers797044908
pharmgkbrs797044908
gwascentralrs797044908
openSNPrs797044908
23andMers797044908
23andMe allrs797044908
SNP Nexus

SNPshotrs797044908
SNPdbers797044908
MSV3drs797044908
GWAS Ctlgrs797044908
Max Magnitude0
ClinVar
Risk rs797044908(AA;AA)
Alt rs797044908(AA;AA)
Reference Rs797044908(TG;TG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene PHF6
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000023.10:g.133551279_133551280delTGinsAA
CLNSRC
CLNACC RCV000190736.1,