rs886039224

Orientation

minus

Stabilized

minus

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

Make rs886039224(A;T)

Make rs886039224(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

19

Position

45414887

Gene

ERCC1

is a	snp
is	mentioned by
dbSNP	rs886039224
dbSNP (classic)	rs886039224
ClinGen	rs886039224
ebi	rs886039224
HLI	rs886039224
Exac	rs886039224
Gnomad	rs886039224
Varsome	rs886039224
LitVar	rs886039224
Map	rs886039224
PheGenI	rs886039224
Biobank	rs886039224
1000 genomes	rs886039224
hgdp	rs886039224
ensembl	rs886039224
geneview	rs886039224
scholar	rs886039224
google	rs886039224
pharmgkb	rs886039224
gwascentral	rs886039224
openSNP	rs886039224
23andMe	rs886039224
SNPshot	rs886039224
SNPdbe	rs886039224
MSV3d	rs886039224
GWAS Ctlg	rs886039224

Max Magnitude

0

ClinVar
Risk	rs886039224(T;T)
Alt	rs886039224(T;T)
Reference	Rs886039224(A;A)
Significance	Pathogenic
Disease	Cockayne syndrome
Variation	info
Gene	ERCC1
CLNDBN	Cockayne syndrome
Reversed	1
HGVS	NC_000019.9:g.45918145T>A
CLNSRC
CLNACC	RCV000247362.1,