rs796052825

Orientation

minus

Stabilized

minus

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

Make rs796052825(-;-)

Make rs796052825(-;ATC)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408295

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052825
dbSNP (classic)	rs796052825
ClinGen	rs796052825
ebi	rs796052825
HLI	rs796052825
Exac	rs796052825
Gnomad	rs796052825
Varsome	rs796052825
LitVar	rs796052825
Map	rs796052825
PheGenI	rs796052825
Biobank	rs796052825
1000 genomes	rs796052825
hgdp	rs796052825
ensembl	rs796052825
geneview	rs796052825
scholar	rs796052825
google	rs796052825
pharmgkb	rs796052825
gwascentral	rs796052825
openSNP	rs796052825
23andMe	rs796052825
SNPshot	rs796052825
SNPdbe	rs796052825
MSV3d	rs796052825
GWAS Ctlg	rs796052825

Max Magnitude

0

ClinVar
Risk	rs796052825(-;-)
Alt	rs796052825(-;-)
Reference	Rs796052825(ATC;ATC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663293_99663295delGAT
CLNSRC
CLNACC	RCV000188385.1,