rs748973032

Orientation

plus

Stabilized

plus

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

Make rs748973032(A;A)

Make rs748973032(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

50524129

Gene	NCAPH2, SCO2

is a	snp
is	mentioned by
dbSNP	rs748973032
dbSNP (classic)	rs748973032
ClinGen	rs748973032
ebi	rs748973032
HLI	rs748973032
Exac	rs748973032
Gnomad	rs748973032
Varsome	rs748973032
LitVar	rs748973032
Map	rs748973032
PheGenI	rs748973032
Biobank	rs748973032
1000 genomes	rs748973032
hgdp	rs748973032
ensembl	rs748973032
geneview	rs748973032
scholar	rs748973032
google	rs748973032
pharmgkb	rs748973032
gwascentral	rs748973032
openSNP	rs748973032
23andMe	rs748973032
SNPshot	rs748973032
SNPdbe	rs748973032
MSV3d	rs748973032
GWAS Ctlg	rs748973032

Max Magnitude

0

ClinVar
Risk	rs748973032(A;A)
Alt	rs748973032(A;A)
Reference	Rs748973032(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NCAPH2 SCO2
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.50962558G>A
CLNSRC
CLNACC	RCV000196635.1,