rs1057520761

Orientation

minus

Stabilized

minus

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

Make rs1057520761(A;A)

Make rs1057520761(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

100407773

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs1057520761
dbSNP (classic)	rs1057520761
ClinGen	rs1057520761
ebi	rs1057520761
HLI	rs1057520761
Exac	rs1057520761
Gnomad	rs1057520761
Varsome	rs1057520761
LitVar	rs1057520761
Map	rs1057520761
PheGenI	rs1057520761
Biobank	rs1057520761
1000 genomes	rs1057520761
hgdp	rs1057520761
ensembl	rs1057520761
geneview	rs1057520761
scholar	rs1057520761
google	rs1057520761
pharmgkb	rs1057520761
gwascentral	rs1057520761
openSNP	rs1057520761
23andMe	rs1057520761
SNPshot	rs1057520761
SNPdbe	rs1057520761
MSV3d	rs1057520761
GWAS Ctlg	rs1057520761

Max Magnitude

0

ClinVar
Risk	rs1057520761(A;A)
Alt	rs1057520761(A;A)
Reference	Rs1057520761(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662771G>T
CLNSRC
CLNACC	RCV000425887.1,