rs863224252

Orientation

minus

Stabilized

minus

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

Make rs863224252(A;A)

Make rs863224252(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

50526609

Gene	SCO2, TYMP

is a	snp
is	mentioned by
dbSNP	rs863224252
dbSNP (classic)	rs863224252
ClinGen	rs863224252
ebi	rs863224252
HLI	rs863224252
Exac	rs863224252
Gnomad	rs863224252
Varsome	rs863224252
LitVar	rs863224252
Map	rs863224252
PheGenI	rs863224252
Biobank	rs863224252
1000 genomes	rs863224252
hgdp	rs863224252
ensembl	rs863224252
geneview	rs863224252
scholar	rs863224252
google	rs863224252
pharmgkb	rs863224252
gwascentral	rs863224252
openSNP	rs863224252
23andMe	rs863224252
SNPshot	rs863224252
SNPdbe	rs863224252
MSV3d	rs863224252
GWAS Ctlg	rs863224252

Max Magnitude

0

ClinVar
Risk	rs863224252(A;A)
Alt	rs863224252(A;A)
Reference	Rs863224252(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TYMP SCO2
CLNDBN	not provided
Reversed	1
HGVS	NC_000022.10:g.50965038G>T
CLNSRC
CLNACC	RCV000197047.1,