rs751831616

Orientation

plus

Stabilized

plus

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

Make rs751831616(C;C)

Make rs751831616(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

102218846

Gene

RRM2B

is a	snp
is	mentioned by
dbSNP	rs751831616
dbSNP (classic)	rs751831616
ClinGen	rs751831616
ebi	rs751831616
HLI	rs751831616
Exac	rs751831616
Gnomad	rs751831616
Varsome	rs751831616
LitVar	rs751831616
Map	rs751831616
PheGenI	rs751831616
Biobank	rs751831616
1000 genomes	rs751831616
hgdp	rs751831616
ensembl	rs751831616
geneview	rs751831616
scholar	rs751831616
google	rs751831616
pharmgkb	rs751831616
gwascentral	rs751831616
openSNP	rs751831616
23andMe	rs751831616
SNPshot	rs751831616
SNPdbe	rs751831616
MSV3d	rs751831616
GWAS Ctlg	rs751831616

Max Magnitude

0

ClinVar
Risk	rs751831616(C;C)
Alt	rs751831616(C;C)
Reference	Rs751831616(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RRM2B
CLNDBN	not provided
Reversed	0
HGVS	NC_000008.10:g.103231074T>C
CLNSRC
CLNACC	RCV000200061.1,