rs863224191

Orientation

minus

Stabilized

minus

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

Make rs863224191(C;T)

Make rs863224191(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102224076

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs863224191
dbSNP (classic)	rs863224191
ClinGen	rs863224191
ebi	rs863224191
HLI	rs863224191
Exac	rs863224191
Gnomad	rs863224191
Varsome	rs863224191
LitVar	rs863224191
Map	rs863224191
PheGenI	rs863224191
Biobank	rs863224191
1000 genomes	rs863224191
hgdp	rs863224191
ensembl	rs863224191
geneview	rs863224191
scholar	rs863224191
google	rs863224191
pharmgkb	rs863224191
gwascentral	rs863224191
openSNP	rs863224191
23andMe	rs863224191
SNPshot	rs863224191
SNPdbe	rs863224191
MSV3d	rs863224191
GWAS Ctlg	rs863224191

Max Magnitude

0

ClinVar
Risk	rs863224191(T;T)
Alt	rs863224191(T;T)
Reference	Rs863224191(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.103236304G>A
CLNSRC
CLNACC	RCV000199844.1,