Have questions? Visit https://www.reddit.com/r/SNPedia

rs2228526

From SNPedia

Orientationminus
Stabilizedminus
Make rs2228526(A;A)
Make rs2228526(A;G)
Make rs2228526(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position49470671
GeneERCC6
is asnp
is mentioned by
dbSNPrs2228526
dbSNP (classic)rs2228526
ClinGenrs2228526
ebirs2228526
HLIrs2228526
Exacrs2228526
Gnomadrs2228526
Varsomers2228526
LitVarrs2228526
Maprs2228526
PheGenIrs2228526
Biobankrs2228526
1000 genomesrs2228526
hgdprs2228526
ensemblrs2228526
geneviewrs2228526
scholarrs2228526
googlers2228526
pharmgkbrs2228526
gwascentralrs2228526
openSNPrs2228526
23andMers2228526
23andMe allrs2228526
SNPshotrs2228526
SNPdbers2228526
MSV3drs2228526
GWAS Ctlgrs2228526
Max Magnitude
? (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