rs863224251

Orientation

minus

Stabilized

minus

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

Make rs863224251(A;T)

Make rs863224251(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

50528552

Gene

TYMP

is a	snp
is	mentioned by
dbSNP	rs863224251
dbSNP (classic)	rs863224251
ClinGen	rs863224251
ebi	rs863224251
HLI	rs863224251
Exac	rs863224251
Gnomad	rs863224251
Varsome	rs863224251
LitVar	rs863224251
Map	rs863224251
PheGenI	rs863224251
Biobank	rs863224251
1000 genomes	rs863224251
hgdp	rs863224251
ensembl	rs863224251
geneview	rs863224251
scholar	rs863224251
google	rs863224251
pharmgkb	rs863224251
gwascentral	rs863224251
openSNP	rs863224251
23andMe	rs863224251
SNPshot	rs863224251
SNPdbe	rs863224251
MSV3d	rs863224251
GWAS Ctlg	rs863224251

Max Magnitude

0

ClinVar
Risk	rs863224251(T;T)
Alt	rs863224251(T;T)
Reference	Rs863224251(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TYMP
CLNDBN	not provided
Reversed	1
HGVS	NC_000022.10:g.50966981T>A
CLNSRC
CLNACC	RCV000200518.1,