rs786205171

Orientation

minus

Stabilized

minus

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

Make rs786205171(-;-)

Make rs786205171(-;A)

Reference

GRCh38.p2 38.2/146

Chromosome

10

Position

49470424

Gene

ERCC6

is a	snp
is	mentioned by
dbSNP	rs786205171
dbSNP (classic)	rs786205171
ClinGen	rs786205171
ebi	rs786205171
HLI	rs786205171
Exac	rs786205171
Gnomad	rs786205171
Varsome	rs786205171
LitVar	rs786205171
Map	rs786205171
PheGenI	rs786205171
Biobank	rs786205171
1000 genomes	rs786205171
hgdp	rs786205171
ensembl	rs786205171
geneview	rs786205171
scholar	rs786205171
google	rs786205171
pharmgkb	rs786205171
gwascentral	rs786205171
openSNP	rs786205171
23andMe	rs786205171
SNPshot	rs786205171
SNPdbe	rs786205171
MSV3d	rs786205171
GWAS Ctlg	rs786205171

Max Magnitude

0

ClinVar
Risk	rs786205171(-;-)
Alt	rs786205171(-;-)
Reference	Rs786205171(A;A)
Significance	Pathogenic
Disease	Cockayne syndrome B not provided
Variation	info
Gene	ERCC6
CLNDBN	Cockayne syndrome B not provided
Reversed	1
HGVS	NC_000010.10:g.50678470delT
CLNSRC
CLNACC	RCV000170386.1, RCV000224382.1,