rs794727710

Orientation

plus

Stabilized

plus

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

Make rs794727710(G;T)

Make rs794727710(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

87714864

Gene

PAPSS2

is a	snp
is	mentioned by
dbSNP	rs794727710
dbSNP (classic)	rs794727710
ClinGen	rs794727710
ebi	rs794727710
HLI	rs794727710
Exac	rs794727710
Gnomad	rs794727710
Varsome	rs794727710
LitVar	rs794727710
Map	rs794727710
PheGenI	rs794727710
Biobank	rs794727710
1000 genomes	rs794727710
hgdp	rs794727710
ensembl	rs794727710
geneview	rs794727710
scholar	rs794727710
google	rs794727710
pharmgkb	rs794727710
gwascentral	rs794727710
openSNP	rs794727710
23andMe	rs794727710
SNPshot	rs794727710
SNPdbe	rs794727710
MSV3d	rs794727710
GWAS Ctlg	rs794727710

Max Magnitude

0

ClinVar
Risk	rs794727710(T;T)
Alt	rs794727710(T;T)
Reference	Rs794727710(G;G)
Significance	Pathogenic
Disease	Spondyloepimetaphyseal dysplasia
Variation	info
Gene	PAPSS2
CLNDBN	Spondyloepimetaphyseal dysplasia, pakistani type
Reversed	0
HGVS	NC_000010.10:g.89474621G>T
CLNSRC
CLNACC	RCV000178816.1,