rs1057518401

Orientation

plus

Stabilized

plus

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

Make rs1057518401(-;AAATGCTGGT)

Make rs1057518401(AAATGCTGGT;AAATGCTGGT)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

76733658

Gene	METTL23, SRSF2

is a	snp
is	mentioned by
dbSNP	rs1057518401
dbSNP (classic)	rs1057518401
ClinGen	rs1057518401
ebi	rs1057518401
HLI	rs1057518401
Exac	rs1057518401
Gnomad	rs1057518401
Varsome	rs1057518401
LitVar	rs1057518401
Map	rs1057518401
PheGenI	rs1057518401
Biobank	rs1057518401
1000 genomes	rs1057518401
hgdp	rs1057518401
ensembl	rs1057518401
geneview	rs1057518401
scholar	rs1057518401
google	rs1057518401
pharmgkb	rs1057518401
gwascentral	rs1057518401
openSNP	rs1057518401
23andMe	rs1057518401
SNPshot	rs1057518401
SNPdbe	rs1057518401
MSV3d	rs1057518401
GWAS Ctlg	rs1057518401

Max Magnitude

0

ClinVar
Risk	rs1057518401(AAATGCTGGT;AAATGCTGGT)
Alt	rs1057518401(AAATGCTGGT;AAATGCTGGT)
Reference	Rs1057518401(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SRSF2 METTL23
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.74729731_74729740dupAAATGCTGGT
CLNSRC
CLNACC	RCV000413581.1,