rs63750262

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;AATG)	6	Lynch syndrome, pathogenic mutation
(I;I)	0

Make rs63750262(AATG;AATG)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47806474

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs63750262
dbSNP (classic)	rs63750262
ClinGen	rs63750262
ebi	rs63750262
HLI	rs63750262
Exac	rs63750262
Gnomad	rs63750262
Varsome	rs63750262
LitVar	rs63750262
Map	rs63750262
PheGenI	rs63750262
Biobank	rs63750262
1000 genomes	rs63750262
hgdp	rs63750262
ensembl	rs63750262
geneview	rs63750262
scholar	rs63750262
google	rs63750262
pharmgkb	rs63750262
gwascentral	rs63750262
openSNP	rs63750262
23andMe	rs63750262
SNPshot	rs63750262
SNPdbe	rs63750262
MSV3d	rs63750262
GWAS Ctlg	rs63750262

Max Magnitude

6

ClinVar
Risk	rs63750262(AATG;AATG)
Alt	rs63750262(AATG;AATG)
Reference	Rs63750262(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033610_48033613dupAATG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074939.2,