rs373498347

Orientation

plus

Stabilized

plus

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

Make rs373498347(C;G)

Make rs373498347(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

21

Position

34880698

Gene	LOC102724584, RUNX1

is a	snp
is	mentioned by
dbSNP	rs373498347
dbSNP (classic)	rs373498347
ClinGen	rs373498347
ebi	rs373498347
HLI	rs373498347
Exac	rs373498347
Gnomad	rs373498347
Varsome	rs373498347
LitVar	rs373498347
Map	rs373498347
PheGenI	rs373498347
Biobank	rs373498347
1000 genomes	rs373498347
hgdp	rs373498347
ensembl	rs373498347
geneview	rs373498347
scholar	rs373498347
google	rs373498347
pharmgkb	rs373498347
gwascentral	rs373498347
openSNP	rs373498347
23andMe	rs373498347
SNPshot	rs373498347
SNPdbe	rs373498347
MSV3d	rs373498347
GWAS Ctlg	rs373498347

Max Magnitude

0

ClinVar
Risk	rs373498347(G;G) rs373498347(T;T)
Alt	rs373498347(G;G) rs373498347(T;T)
Reference	Rs373498347(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RUNX1
CLNDBN	not provided
Reversed	0
HGVS	NC_000021.8:g.36252995C>G
CLNSRC
CLNACC	RCV000493659.1,