rs786205168

Orientation

minus

Stabilized

minus

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

Make rs786205168(-;-)

Make rs786205168(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

49505892

Gene

ERCC6

is a	snp
is	mentioned by
dbSNP	rs786205168
dbSNP (classic)	rs786205168
ClinGen	rs786205168
ebi	rs786205168
HLI	rs786205168
Exac	rs786205168
Gnomad	rs786205168
Varsome	rs786205168
LitVar	rs786205168
Map	rs786205168
PheGenI	rs786205168
Biobank	rs786205168
1000 genomes	rs786205168
hgdp	rs786205168
ensembl	rs786205168
geneview	rs786205168
scholar	rs786205168
google	rs786205168
pharmgkb	rs786205168
gwascentral	rs786205168
openSNP	rs786205168
23andMe	rs786205168
SNPshot	rs786205168
SNPdbe	rs786205168
MSV3d	rs786205168
GWAS Ctlg	rs786205168

Max Magnitude

0

ClinVar
Risk	rs786205168(-;-)
Alt	rs786205168(-;-)
Reference	Rs786205168(G;G)
Significance	Probable-Pathogenic
Disease	Cockayne syndrome B
Variation	info
Gene	ERCC6
CLNDBN	Cockayne syndrome B
Reversed	1
HGVS	NC_000010.10:g.50713938delC
CLNSRC
CLNACC	RCV000170368.1,