rs1057524751

Orientation

minus

Stabilized

minus

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

Make rs1057524751(G;T)

Make rs1057524751(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

100407799

Gene

PCDH19

is a	snp
is	mentioned by
dbSNP	rs1057524751
dbSNP (classic)	rs1057524751
ClinGen	rs1057524751
ebi	rs1057524751
HLI	rs1057524751
Exac	rs1057524751
Gnomad	rs1057524751
Varsome	rs1057524751
LitVar	rs1057524751
Map	rs1057524751
PheGenI	rs1057524751
Biobank	rs1057524751
1000 genomes	rs1057524751
hgdp	rs1057524751
ensembl	rs1057524751
geneview	rs1057524751
scholar	rs1057524751
google	rs1057524751
pharmgkb	rs1057524751
gwascentral	rs1057524751
openSNP	rs1057524751
23andMe	rs1057524751
SNPshot	rs1057524751
SNPdbe	rs1057524751
MSV3d	rs1057524751
GWAS Ctlg	rs1057524751

Max Magnitude

0

ClinVar
Risk	rs1057524751(T;T)
Alt	rs1057524751(T;T)
Reference	Rs1057524751(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PCDH19
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.99662797C>A
CLNSRC
CLNACC	RCV000431864.1,