rs398124428

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs398124428(G;T)

Make rs398124428(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

134377620

Gene

PHF6

is a	snp
is	mentioned by
dbSNP	rs398124428
dbSNP (classic)	rs398124428
ClinGen	rs398124428
ebi	rs398124428
HLI	rs398124428
Exac	rs398124428
Gnomad	rs398124428
Varsome	rs398124428
LitVar	rs398124428
Map	rs398124428
PheGenI	rs398124428
Biobank	rs398124428
1000 genomes	rs398124428
hgdp	rs398124428
ensembl	rs398124428
geneview	rs398124428
scholar	rs398124428
google	rs398124428
pharmgkb	rs398124428
gwascentral	rs398124428
openSNP	rs398124428
23andMe	rs398124428
SNPshot	rs398124428
SNPdbe	rs398124428
MSV3d	rs398124428
GWAS Ctlg	rs398124428

Max Magnitude

0

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,