rs1057524103

Orientation

minus

Stabilized

minus

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

Make rs1057524103(A;A)

Make rs1057524103(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

115997195

Gene

MED13L

is a	snp
is	mentioned by
dbSNP	rs1057524103
dbSNP (classic)	rs1057524103
ClinGen	rs1057524103
ebi	rs1057524103
HLI	rs1057524103
Exac	rs1057524103
Gnomad	rs1057524103
Varsome	rs1057524103
LitVar	rs1057524103
Map	rs1057524103
PheGenI	rs1057524103
Biobank	rs1057524103
1000 genomes	rs1057524103
hgdp	rs1057524103
ensembl	rs1057524103
geneview	rs1057524103
scholar	rs1057524103
google	rs1057524103
pharmgkb	rs1057524103
gwascentral	rs1057524103
openSNP	rs1057524103
23andMe	rs1057524103
SNPshot	rs1057524103
SNPdbe	rs1057524103
MSV3d	rs1057524103
GWAS Ctlg	rs1057524103

Max Magnitude

0

ClinVar
Risk	rs1057524103(A;A)
Alt	rs1057524103(A;A)
Reference	Rs1057524103(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MED13L
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.116435000G>T
CLNSRC
CLNACC	RCV000429083.1,