rs2228526

Orientation

minus

Stabilized

minus

Make rs2228526(A;A)

Make rs2228526(A;G)

Make rs2228526(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

49470671

Gene

ERCC6

is a	snp
is	mentioned by
dbSNP	rs2228526
dbSNP (classic)	rs2228526
ClinGen	rs2228526
ebi	rs2228526
HLI	rs2228526
Exac	rs2228526
Gnomad	rs2228526
Varsome	rs2228526
LitVar	rs2228526
Map	rs2228526
PheGenI	rs2228526
Biobank	rs2228526
1000 genomes	rs2228526
hgdp	rs2228526
ensembl	rs2228526
geneview	rs2228526
scholar	rs2228526
google	rs2228526
pharmgkb	rs2228526
gwascentral	rs2228526
openSNP	rs2228526
23andMe	rs2228526
SNPshot	rs2228526
SNPdbe	rs2228526
MSV3d	rs2228526
GWAS Ctlg	rs2228526

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 28707579] The Involvement of ERCC2/XPD and ERCC6/CSB Wild Type Alleles in Protection against Aging and Cancer.

ClinVar
Risk	rs2228526(G;G)
Alt	rs2228526(G;G)
Reference	rs2228526(A;A)
Significance	Other
Disease	not specified Cockayne syndrome Cerebrooculofacioskeletal Syndrome Macular degeneration
Variation	info
Gene	ERCC6
CLNDBN	not specified Cockayne syndrome Cerebrooculofacioskeletal Syndrome Macular degeneration
Reversed	1
HGVS	NC_000010.10:g.50678717T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000116997.6, RCV000287947.1, RCV000322054.1, RCV000378942.1,

[PMID 29151331] Polymorphisms of cancer-related genes and risk of multipleprimary malignancies involving colorectal cancer