rs878853739

Orientation

plus

Stabilized

plus

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

Make rs878853739(-;A)

Make rs878853739(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806514

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs878853739
dbSNP (classic)	rs878853739
ClinGen	rs878853739
ebi	rs878853739
HLI	rs878853739
Exac	rs878853739
Gnomad	rs878853739
Varsome	rs878853739
LitVar	rs878853739
Map	rs878853739
PheGenI	rs878853739
Biobank	rs878853739
1000 genomes	rs878853739
hgdp	rs878853739
ensembl	rs878853739
geneview	rs878853739
scholar	rs878853739
google	rs878853739
pharmgkb	rs878853739
gwascentral	rs878853739
openSNP	rs878853739
23andMe	rs878853739
SNPshot	rs878853739
SNPdbe	rs878853739
MSV3d	rs878853739
GWAS Ctlg	rs878853739

Max Magnitude

0

ClinVar
Risk	rs878853739(A;A)
Alt	rs878853739(A;A)
Reference	Rs878853739(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033653dupA
CLNSRC
CLNACC	RCV000230977.2,