rs796052807

Orientation

minus

Stabilized

minus

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

Make rs796052807(A;A)

Make rs796052807(A;T)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100407902

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052807
dbSNP (classic)	rs796052807
ClinGen	rs796052807
ebi	rs796052807
HLI	rs796052807
Exac	rs796052807
Gnomad	rs796052807
Varsome	rs796052807
LitVar	rs796052807
Map	rs796052807
PheGenI	rs796052807
Biobank	rs796052807
1000 genomes	rs796052807
hgdp	rs796052807
ensembl	rs796052807
geneview	rs796052807
scholar	rs796052807
google	rs796052807
pharmgkb	rs796052807
gwascentral	rs796052807
openSNP	rs796052807
23andMe	rs796052807
SNPshot	rs796052807
SNPdbe	rs796052807
MSV3d	rs796052807
GWAS Ctlg	rs796052807

Max Magnitude

0

ClinVar
Risk	rs796052807(A;A)
Alt	rs796052807(A;A)
Reference	Rs796052807(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662900A>T
CLNSRC
CLNACC	RCV000188358.2,