rs796052830

Orientation

minus

Stabilized

minus

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

Make rs796052830(-;-)

Make rs796052830(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407464

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052830
dbSNP (classic)	rs796052830
ClinGen	rs796052830
ebi	rs796052830
HLI	rs796052830
Exac	rs796052830
Gnomad	rs796052830
Varsome	rs796052830
LitVar	rs796052830
Map	rs796052830
PheGenI	rs796052830
Biobank	rs796052830
1000 genomes	rs796052830
hgdp	rs796052830
ensembl	rs796052830
geneview	rs796052830
scholar	rs796052830
google	rs796052830
pharmgkb	rs796052830
gwascentral	rs796052830
openSNP	rs796052830
23andMe	rs796052830
SNPshot	rs796052830
SNPdbe	rs796052830
MSV3d	rs796052830
GWAS Ctlg	rs796052830

Max Magnitude

0

ClinVar
Risk	rs796052830(-;-)
Alt	rs796052830(-;-)
Reference	Rs796052830(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662462delT
CLNSRC
CLNACC	RCV000188391.1,