rs768265778

Orientation

plus

Stabilized

plus

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

Make rs768265778(-;-)

Make rs768265778(-;CTACTCATGGTGAGGGAGCT)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

65558613

is a	snp
is	mentioned by
dbSNP	rs768265778
dbSNP (classic)	rs768265778
ClinGen	rs768265778
ebi	rs768265778
HLI	rs768265778
Exac	rs768265778
Gnomad	rs768265778
Varsome	rs768265778
LitVar	rs768265778
Map	rs768265778
PheGenI	rs768265778
Biobank	rs768265778
1000 genomes	rs768265778
hgdp	rs768265778
ensembl	rs768265778
geneview	rs768265778
scholar	rs768265778
google	rs768265778
pharmgkb	rs768265778
gwascentral	rs768265778
openSNP	rs768265778
23andMe	rs768265778
SNPshot	rs768265778
SNPdbe	rs768265778
MSV3d	rs768265778
GWAS Ctlg	rs768265778

Max Magnitude

0

Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in [PMID 26681312]

ClinVar
Risk	rs768265778(-;-)
Alt	rs768265778(-;-)
Reference	Rs768265778(CTACTCATGGTGAGGGAGCT;CTACTCATGGTGAGGGAGCT)
Significance	Unknown
Disease	Oligodontia-colorectal cancer syndrome
Variation	info
Gene
CLNDBN	Oligodontia-colorectal cancer syndrome
Reversed	0
HGVS	NC_000017.10:g.63554731_63554750del20
CLNSRC
CLNACC	RCV000228766.1,