rs398123241

Orientation

plus

Stabilized

plus

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

Make rs398123241(A;A)

Make rs398123241(A;G)

Reference

GRCh38 38.1/141

Chromosome

X

Position

134498389

Gene

HPRT1

is a	snp
is	mentioned by
dbSNP	rs398123241
dbSNP (classic)	rs398123241
ClinGen	rs398123241
ebi	rs398123241
HLI	rs398123241
Exac	rs398123241
Gnomad	rs398123241
Varsome	rs398123241
LitVar	rs398123241
Map	rs398123241
PheGenI	rs398123241
Biobank	rs398123241
1000 genomes	rs398123241
hgdp	rs398123241
ensembl	rs398123241
geneview	rs398123241
scholar	rs398123241
google	rs398123241
pharmgkb	rs398123241
gwascentral	rs398123241
openSNP	rs398123241
23andMe	rs398123241
SNPshot	rs398123241
SNPdbe	rs398123241
MSV3d	rs398123241
GWAS Ctlg	rs398123241

Max Magnitude

0

ClinVar
Risk	rs398123241(A;A)
Alt	rs398123241(A;A)
Reference	Rs398123241(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HPRT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.133632419G>A
CLNSRC	HGMD
CLNACC	RCV000078345.4,