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rs398124428

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124428(G;T)
Make rs398124428(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position134377620
GenePHF6
is asnp
is mentioned by
dbSNPrs398124428
ebirs398124428
HLIrs398124428
Exacrs398124428
Varsomers398124428
Maprs398124428
PheGenIrs398124428
hapmaprs398124428
1000 genomesrs398124428
hgdprs398124428
ensemblrs398124428
gopubmedrs398124428
geneviewrs398124428
scholarrs398124428
googlers398124428
pharmgkbrs398124428
gwascentralrs398124428
openSNPrs398124428
23andMers398124428
23andMe allrs398124428
SNP Nexus

SNPshotrs398124428
SNPdbers398124428
MSV3drs398124428
GWAS Ctlgrs398124428
Max Magnitude0
ClinVar
Risk rs398124428(T;T)
Alt rs398124428(T;T)
Reference rs398124428(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PHF6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.133511650G>T
CLNSRC ClinVar Emory University
CLNACC RCV000082301.4,