rs863224877

Orientation

minus

Stabilized

minus

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

Make rs863224877(A;G)

Make rs863224877(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

72351840

Gene

HDAC8

is a	snp
is	mentioned by
dbSNP	rs863224877
dbSNP (classic)	rs863224877
ClinGen	rs863224877
ebi	rs863224877
HLI	rs863224877
Exac	rs863224877
Gnomad	rs863224877
Varsome	rs863224877
LitVar	rs863224877
Map	rs863224877
PheGenI	rs863224877
Biobank	rs863224877
1000 genomes	rs863224877
hgdp	rs863224877
ensembl	rs863224877
geneview	rs863224877
scholar	rs863224877
google	rs863224877
pharmgkb	rs863224877
gwascentral	rs863224877
openSNP	rs863224877
23andMe	rs863224877
SNPshot	rs863224877
SNPdbe	rs863224877
MSV3d	rs863224877
GWAS Ctlg	rs863224877

Max Magnitude

0

ClinVar
Risk	rs863224877(G;G)
Alt	rs863224877(G;G)
Reference	Rs863224877(A;A)
Significance	Probable-Pathogenic
Disease	Cornelia de Lange syndrome 5
Variation	info
Gene	HDAC8
CLNDBN	Cornelia de Lange syndrome 5
Reversed	1
HGVS	NC_000023.10:g.71571690T>C
CLNSRC
CLNACC	RCV000196804.1,