rs767083273

Orientation

plus

Stabilized

plus

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

Make rs767083273(C;T)

Make rs767083273(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

104053064

Gene

COL17A1

is a	snp
is	mentioned by
dbSNP	rs767083273
dbSNP (classic)	rs767083273
ClinGen	rs767083273
ebi	rs767083273
HLI	rs767083273
Exac	rs767083273
Gnomad	rs767083273
Varsome	rs767083273
LitVar	rs767083273
Map	rs767083273
PheGenI	rs767083273
Biobank	rs767083273
1000 genomes	rs767083273
hgdp	rs767083273
ensembl	rs767083273
geneview	rs767083273
scholar	rs767083273
google	rs767083273
pharmgkb	rs767083273
gwascentral	rs767083273
openSNP	rs767083273
23andMe	rs767083273
SNPshot	rs767083273
SNPdbe	rs767083273
MSV3d	rs767083273
GWAS Ctlg	rs767083273

Max Magnitude

0

ClinVar
Risk	rs767083273(G;G) rs767083273(T;T)
Alt	rs767083273(G;G) rs767083273(T;T)
Reference	Rs767083273(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	COL17A1
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.105812822C>T
CLNSRC
CLNACC	RCV000427953.1,