rs796052795

Orientation

minus

Stabilized

minus

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

Make rs796052795(C;C)

Make rs796052795(C;G)

Reference

GRCh38.p2 38.2/147

Chromosome

X

Position

100408237

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs796052795
dbSNP (classic)	rs796052795
ClinGen	rs796052795
ebi	rs796052795
HLI	rs796052795
Exac	rs796052795
Gnomad	rs796052795
Varsome	rs796052795
LitVar	rs796052795
Map	rs796052795
PheGenI	rs796052795
Biobank	rs796052795
1000 genomes	rs796052795
hgdp	rs796052795
ensembl	rs796052795
geneview	rs796052795
scholar	rs796052795
google	rs796052795
pharmgkb	rs796052795
gwascentral	rs796052795
openSNP	rs796052795
23andMe	rs796052795
SNPshot	rs796052795
SNPdbe	rs796052795
MSV3d	rs796052795
GWAS Ctlg	rs796052795

Max Magnitude

0

ClinVar
Risk	rs796052795(A;A) rs796052795(C;C)
Alt	rs796052795(A;A) rs796052795(C;C)
Reference	Rs796052795(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99663235C>G; NC_000023.10:g.99663235C>T
CLNSRC
CLNACC	RCV000188345.1, RCV000489751.1,