rs797044867

Orientation

minus

Stabilized

minus

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

Make rs797044867(A;A)

Make rs797044867(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

110178196

Gene

COL4A1

is a	snp
is	mentioned by
dbSNP	rs797044867
dbSNP (classic)	rs797044867
ClinGen	rs797044867
ebi	rs797044867
HLI	rs797044867
Exac	rs797044867
Gnomad	rs797044867
Varsome	rs797044867
LitVar	rs797044867
Map	rs797044867
PheGenI	rs797044867
Biobank	rs797044867
1000 genomes	rs797044867
hgdp	rs797044867
ensembl	rs797044867
geneview	rs797044867
scholar	rs797044867
google	rs797044867
pharmgkb	rs797044867
gwascentral	rs797044867
openSNP	rs797044867
23andMe	rs797044867
SNPshot	rs797044867
SNPdbe	rs797044867
MSV3d	rs797044867
GWAS Ctlg	rs797044867

Max Magnitude

0

ClinVar
Risk	rs797044867(A;A)
Alt	rs797044867(A;A)
Reference	Rs797044867(G;G)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	COL4A1
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000013.10:g.110830543C>T
CLNSRC
CLNACC	RCV000190674.1,