rs1064795068

Orientation

minus

Stabilized

minus

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

Chromosome

12

Position

115997164

Gene

MED13L

is a	snp
is	mentioned by
dbSNP	rs1064795068
dbSNP (classic)	rs1064795068
ClinGen	rs1064795068
ebi	rs1064795068
HLI	rs1064795068
Exac	rs1064795068
Gnomad	rs1064795068
Varsome	rs1064795068
LitVar	rs1064795068
Map	rs1064795068
PheGenI	rs1064795068
Biobank	rs1064795068
1000 genomes	rs1064795068
hgdp	rs1064795068
ensembl	rs1064795068
geneview	rs1064795068
scholar	rs1064795068
google	rs1064795068
pharmgkb	rs1064795068
gwascentral	rs1064795068
openSNP	rs1064795068
23andMe	rs1064795068
SNPshot	rs1064795068
SNPdbe	rs1064795068
MSV3d	rs1064795068
GWAS Ctlg	rs1064795068

Max Magnitude

0

ClinVar
Risk	rs1064795068(T;T)
Alt	rs1064795068(T;T)
Reference	Rs1064795068(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MED13L
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.116434969G>A
CLNSRC
CLNACC	RCV000483885.1,