rs863223711

Orientation

plus

Stabilized

plus

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

Make rs863223711(C;T)

Make rs863223711(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

71118818

Gene

MED12

is a	snp
is	mentioned by
dbSNP	rs863223711
dbSNP (classic)	rs863223711
ClinGen	rs863223711
ebi	rs863223711
HLI	rs863223711
Exac	rs863223711
Gnomad	rs863223711
Varsome	rs863223711
LitVar	rs863223711
Map	rs863223711
PheGenI	rs863223711
Biobank	rs863223711
1000 genomes	rs863223711
hgdp	rs863223711
ensembl	rs863223711
geneview	rs863223711
scholar	rs863223711
google	rs863223711
pharmgkb	rs863223711
gwascentral	rs863223711
openSNP	rs863223711
23andMe	rs863223711
SNPshot	rs863223711
SNPdbe	rs863223711
MSV3d	rs863223711
GWAS Ctlg	rs863223711

Max Magnitude

0

ClinVar
Risk	rs863223711(T;T)
Alt	rs863223711(T;T)
Reference	Rs863223711(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MED12
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.70338668C>T
CLNSRC
CLNACC	RCV000200077.1,