rs863224194

Orientation

minus

Stabilized

minus

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

Make rs863224194(A;G)

Make rs863224194(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102226036

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs863224194
dbSNP (classic)	rs863224194
ClinGen	rs863224194
ebi	rs863224194
HLI	rs863224194
Exac	rs863224194
Gnomad	rs863224194
Varsome	rs863224194
LitVar	rs863224194
Map	rs863224194
PheGenI	rs863224194
Biobank	rs863224194
1000 genomes	rs863224194
hgdp	rs863224194
ensembl	rs863224194
geneview	rs863224194
scholar	rs863224194
google	rs863224194
pharmgkb	rs863224194
gwascentral	rs863224194
openSNP	rs863224194
23andMe	rs863224194
SNPshot	rs863224194
SNPdbe	rs863224194
MSV3d	rs863224194
GWAS Ctlg	rs863224194

Max Magnitude

0

ClinVar
Risk	rs863224194(G;G)
Alt	rs863224194(G;G)
Reference	Rs863224194(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.103238264T>C
CLNSRC
CLNACC	RCV000200520.2,