rs863223697

Orientation

plus

Stabilized

plus

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

Make rs863223697(C;T)

Make rs863223697(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

71132164

Gene

MED12

is a	snp
is	mentioned by
dbSNP	rs863223697
dbSNP (classic)	rs863223697
ClinGen	rs863223697
ebi	rs863223697
HLI	rs863223697
Exac	rs863223697
Gnomad	rs863223697
Varsome	rs863223697
LitVar	rs863223697
Map	rs863223697
PheGenI	rs863223697
Biobank	rs863223697
1000 genomes	rs863223697
hgdp	rs863223697
ensembl	rs863223697
geneview	rs863223697
scholar	rs863223697
google	rs863223697
pharmgkb	rs863223697
gwascentral	rs863223697
openSNP	rs863223697
23andMe	rs863223697
SNPshot	rs863223697
SNPdbe	rs863223697
MSV3d	rs863223697
GWAS Ctlg	rs863223697

Max Magnitude

0

ClinVar
Risk	rs863223697(T;T)
Alt	rs863223697(T;T)
Reference	Rs863223697(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MED12
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.70352014C>T
CLNSRC
CLNACC	RCV000197941.1,