rs1057520056

Orientation

minus

Stabilized

minus

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

Make rs1057520056(A;A)

Make rs1057520056(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

115997209

Gene

MED13L

is a	snp
is	mentioned by
dbSNP	rs1057520056
dbSNP (classic)	rs1057520056
ClinGen	rs1057520056
ebi	rs1057520056
HLI	rs1057520056
Exac	rs1057520056
Gnomad	rs1057520056
Varsome	rs1057520056
LitVar	rs1057520056
Map	rs1057520056
PheGenI	rs1057520056
Biobank	rs1057520056
1000 genomes	rs1057520056
hgdp	rs1057520056
ensembl	rs1057520056
geneview	rs1057520056
scholar	rs1057520056
google	rs1057520056
pharmgkb	rs1057520056
gwascentral	rs1057520056
openSNP	rs1057520056
23andMe	rs1057520056
SNPshot	rs1057520056
SNPdbe	rs1057520056
MSV3d	rs1057520056
GWAS Ctlg	rs1057520056

Max Magnitude

0

ClinVar
Risk	rs1057520056(A;A)
Alt	rs1057520056(A;A)
Reference	Rs1057520056(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MED13L
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.116435014A>T
CLNSRC
CLNACC	RCV000427272.1,