rs1057520775

Orientation

minus

Stabilized

minus

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

Make rs1057520775(G;T)

Make rs1057520775(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

116277089

Gene

MED13L

is a	snp
is	mentioned by
dbSNP	rs1057520775
dbSNP (classic)	rs1057520775
ClinGen	rs1057520775
ebi	rs1057520775
HLI	rs1057520775
Exac	rs1057520775
Gnomad	rs1057520775
Varsome	rs1057520775
LitVar	rs1057520775
Map	rs1057520775
PheGenI	rs1057520775
Biobank	rs1057520775
1000 genomes	rs1057520775
hgdp	rs1057520775
ensembl	rs1057520775
geneview	rs1057520775
scholar	rs1057520775
google	rs1057520775
pharmgkb	rs1057520775
gwascentral	rs1057520775
openSNP	rs1057520775
23andMe	rs1057520775
SNPshot	rs1057520775
SNPdbe	rs1057520775
MSV3d	rs1057520775
GWAS Ctlg	rs1057520775

Max Magnitude

0

ClinVar
Risk	rs1057520775(T;T)
Alt	rs1057520775(T;T)
Reference	Rs1057520775(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MED13L
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.116714894C>A
CLNSRC
CLNACC	RCV000423089.1,