rs863224255

Orientation

minus

Stabilized

minus

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

Make rs863224255(A;A)

Make rs863224255(A;C)

Reference

GRCh38.p2 38.2/147

Chromosome

22

Position

50529162

Gene

TYMP

is a	snp
is	mentioned by
dbSNP	rs863224255
dbSNP (classic)	rs863224255
ClinGen	rs863224255
ebi	rs863224255
HLI	rs863224255
Exac	rs863224255
Gnomad	rs863224255
Varsome	rs863224255
LitVar	rs863224255
Map	rs863224255
PheGenI	rs863224255
Biobank	rs863224255
1000 genomes	rs863224255
hgdp	rs863224255
ensembl	rs863224255
geneview	rs863224255
scholar	rs863224255
google	rs863224255
pharmgkb	rs863224255
gwascentral	rs863224255
openSNP	rs863224255
23andMe	rs863224255
SNPshot	rs863224255
SNPdbe	rs863224255
MSV3d	rs863224255
GWAS Ctlg	rs863224255

Max Magnitude

0

ClinVar
Risk	rs863224255(A;A)
Alt	rs863224255(A;A)
Reference	Rs863224255(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TYMP
CLNDBN	not provided
Reversed	1
HGVS	NC_000022.10:g.50967591G>T
CLNSRC
CLNACC	RCV000195809.1,