rs727503964

Orientation

plus

Stabilized

plus

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

Make rs727503964(G;G)

Make rs727503964(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

134498438

Gene

HPRT1

is a	snp
is	mentioned by
dbSNP	rs727503964
dbSNP (classic)	rs727503964
ClinGen	rs727503964
ebi	rs727503964
HLI	rs727503964
Exac	rs727503964
Gnomad	rs727503964
Varsome	rs727503964
LitVar	rs727503964
Map	rs727503964
PheGenI	rs727503964
Biobank	rs727503964
1000 genomes	rs727503964
hgdp	rs727503964
ensembl	rs727503964
geneview	rs727503964
scholar	rs727503964
google	rs727503964
pharmgkb	rs727503964
gwascentral	rs727503964
openSNP	rs727503964
23andMe	rs727503964
SNPshot	rs727503964
SNPdbe	rs727503964
MSV3d	rs727503964
GWAS Ctlg	rs727503964

Max Magnitude

0

ClinVar
Risk	rs727503964(G;G)
Alt	rs727503964(G;G)
Reference	Rs727503964(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	HPRT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.133632468T>G
CLNSRC
CLNACC	RCV000153368.3,