rs863224193

Orientation

minus

Stabilized

minus

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

Make rs863224193(A;G)

Make rs863224193(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102218836

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs863224193
dbSNP (classic)	rs863224193
ClinGen	rs863224193
ebi	rs863224193
HLI	rs863224193
Exac	rs863224193
Gnomad	rs863224193
Varsome	rs863224193
LitVar	rs863224193
Map	rs863224193
PheGenI	rs863224193
Biobank	rs863224193
1000 genomes	rs863224193
hgdp	rs863224193
ensembl	rs863224193
geneview	rs863224193
scholar	rs863224193
google	rs863224193
pharmgkb	rs863224193
gwascentral	rs863224193
openSNP	rs863224193
23andMe	rs863224193
SNPshot	rs863224193
SNPdbe	rs863224193
MSV3d	rs863224193
GWAS Ctlg	rs863224193

Max Magnitude

0

ClinVar
Risk	rs863224193(G;G)
Alt	rs863224193(G;G)
Reference	Rs863224193(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.103231064T>C
CLNSRC
CLNACC	RCV000196496.2,