rs863224192

Orientation

minus

Stabilized

minus

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

Make rs863224192(A;A)

Make rs863224192(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102218899

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs863224192
dbSNP (classic)	rs863224192
ClinGen	rs863224192
ebi	rs863224192
HLI	rs863224192
Exac	rs863224192
Gnomad	rs863224192
Varsome	rs863224192
LitVar	rs863224192
Map	rs863224192
PheGenI	rs863224192
Biobank	rs863224192
1000 genomes	rs863224192
hgdp	rs863224192
ensembl	rs863224192
geneview	rs863224192
scholar	rs863224192
google	rs863224192
pharmgkb	rs863224192
gwascentral	rs863224192
openSNP	rs863224192
23andMe	rs863224192
SNPshot	rs863224192
SNPdbe	rs863224192
MSV3d	rs863224192
GWAS Ctlg	rs863224192

Max Magnitude

0

ClinVar
Risk	rs863224192(A;A)
Alt	rs863224192(A;A)
Reference	Rs863224192(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.103231127C>T
CLNSRC
CLNACC	RCV000196346.1,