rs863225420

Orientation

plus

Stabilized

plus

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

Make rs863225420(C;G)

Make rs863225420(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47806805

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs863225420
dbSNP (classic)	rs863225420
ClinGen	rs863225420
ebi	rs863225420
HLI	rs863225420
Exac	rs863225420
Gnomad	rs863225420
Varsome	rs863225420
LitVar	rs863225420
Map	rs863225420
PheGenI	rs863225420
Biobank	rs863225420
1000 genomes	rs863225420
hgdp	rs863225420
ensembl	rs863225420
geneview	rs863225420
scholar	rs863225420
google	rs863225420
pharmgkb	rs863225420
gwascentral	rs863225420
openSNP	rs863225420
23andMe	rs863225420
SNPshot	rs863225420
SNPdbe	rs863225420
MSV3d	rs863225420
GWAS Ctlg	rs863225420

Max Magnitude

0

ClinVar
Risk	rs863225420(G;G)
Alt	rs863225420(G;G)
Reference	Rs863225420(C;C)
Significance	Pathogenic
Disease	not provided Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	not provided Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033944C>G
CLNSRC
CLNACC	RCV000202283.1, RCV000204963.1,