rs769211787

Orientation

plus

Stabilized

plus

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

Make rs769211787(A;C)

Make rs769211787(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

X

Position

108157002

Gene

COL4A6

is a	snp
is	mentioned by
dbSNP	rs769211787
dbSNP (classic)	rs769211787
ClinGen	rs769211787
ebi	rs769211787
HLI	rs769211787
Exac	rs769211787
Gnomad	rs769211787
Varsome	rs769211787
LitVar	rs769211787
Map	rs769211787
PheGenI	rs769211787
Biobank	rs769211787
1000 genomes	rs769211787
hgdp	rs769211787
ensembl	rs769211787
geneview	rs769211787
scholar	rs769211787
google	rs769211787
pharmgkb	rs769211787
gwascentral	rs769211787
openSNP	rs769211787
23andMe	rs769211787
SNPshot	rs769211787
SNPdbe	rs769211787
MSV3d	rs769211787
GWAS Ctlg	rs769211787

Max Magnitude

0

ClinVar
Risk	rs769211787(C;C)
Alt	rs769211787(C;C)
Reference	Rs769211787(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	COL4A6
CLNDBN	not provided
Reversed	0
HGVS	NC_000023.10:g.107400232A>C
CLNSRC
CLNACC	RCV000171443.1,