rs748559929

Orientation

plus

Stabilized

plus

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

Make rs748559929(C;T)

Make rs748559929(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

50526241

Gene	SCO2, TYMP

is a	snp
is	mentioned by
dbSNP	rs748559929
dbSNP (classic)	rs748559929
ClinGen	rs748559929
ebi	rs748559929
HLI	rs748559929
Exac	rs748559929
Gnomad	rs748559929
Varsome	rs748559929
LitVar	rs748559929
Map	rs748559929
PheGenI	rs748559929
Biobank	rs748559929
1000 genomes	rs748559929
hgdp	rs748559929
ensembl	rs748559929
geneview	rs748559929
scholar	rs748559929
google	rs748559929
pharmgkb	rs748559929
gwascentral	rs748559929
openSNP	rs748559929
23andMe	rs748559929
SNPshot	rs748559929
SNPdbe	rs748559929
MSV3d	rs748559929
GWAS Ctlg	rs748559929

Max Magnitude

0

ClinVar
Risk	rs748559929(G;G) rs748559929(T;T)
Alt	rs748559929(G;G) rs748559929(T;T)
Reference	Rs748559929(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SCO2 TYMP
CLNDBN	not provided
Reversed	0
HGVS	NC_000022.10:g.50964670C>T
CLNSRC
CLNACC	RCV000196301.2,