rs61760163

Orientation

plus

Stabilized

plus

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

Make rs61760163(A;A)

Make rs61760163(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

49482860

Gene

ERCC6

is a	snp
is	mentioned by
dbSNP	rs61760163
dbSNP (classic)	rs61760163
ClinGen	rs61760163
ebi	rs61760163
HLI	rs61760163
Exac	rs61760163
Gnomad	rs61760163
Varsome	rs61760163
LitVar	rs61760163
Map	rs61760163
PheGenI	rs61760163
Biobank	rs61760163
1000 genomes	rs61760163
hgdp	rs61760163
ensembl	rs61760163
geneview	rs61760163
scholar	rs61760163
google	rs61760163
pharmgkb	rs61760163
gwascentral	rs61760163
openSNP	rs61760163
23andMe	rs61760163
SNPshot	rs61760163
SNPdbe	rs61760163
MSV3d	rs61760163
GWAS Ctlg	rs61760163

Max Magnitude

0

ClinVar
Risk	rs61760163(A;A)
Alt	rs61760163(A;A)
Reference	Rs61760163(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Cerebrooculofacioskeletal Syndrome Cockayne syndrome Macular degeneration
Variation	info
Gene	ERCC6
CLNDBN	not specified Cerebrooculofacioskeletal Syndrome Cockayne syndrome Macular degeneration
Reversed	0
HGVS	NC_000010.10:g.50690906G>A
CLNSRC
CLNACC	RCV000170374.3, RCV000289884.1, RCV000344840.1, RCV000384253.1,