rs1057521913

Orientation

plus

Stabilized

plus

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

Make rs1057521913(C;C)

Make rs1057521913(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

76733378

Gene

METTL23

is a	snp
is	mentioned by
dbSNP	rs1057521913
dbSNP (classic)	rs1057521913
ClinGen	rs1057521913
ebi	rs1057521913
HLI	rs1057521913
Exac	rs1057521913
Gnomad	rs1057521913
Varsome	rs1057521913
LitVar	rs1057521913
Map	rs1057521913
PheGenI	rs1057521913
Biobank	rs1057521913
1000 genomes	rs1057521913
hgdp	rs1057521913
ensembl	rs1057521913
geneview	rs1057521913
scholar	rs1057521913
google	rs1057521913
pharmgkb	rs1057521913
gwascentral	rs1057521913
openSNP	rs1057521913
23andMe	rs1057521913
SNPshot	rs1057521913
SNPdbe	rs1057521913
MSV3d	rs1057521913
GWAS Ctlg	rs1057521913

Max Magnitude

0

ClinVar
Risk	rs1057521913(C;C)
Alt	rs1057521913(C;C)
Reference	Rs1057521913(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	METTL23
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.74729460G>C
CLNSRC
CLNACC	RCV000421646.1,