rs863224476

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;A)	6	Lynch syndrome
(A;A)	0	common in clinvar

Make rs863224476(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47803682

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs863224476
dbSNP (classic)	rs863224476
ClinGen	rs863224476
ebi	rs863224476
HLI	rs863224476
Exac	rs863224476
Gnomad	rs863224476
Varsome	rs863224476
LitVar	rs863224476
Map	rs863224476
PheGenI	rs863224476
Biobank	rs863224476
1000 genomes	rs863224476
hgdp	rs863224476
ensembl	rs863224476
geneview	rs863224476
scholar	rs863224476
google	rs863224476
pharmgkb	rs863224476
gwascentral	rs863224476
openSNP	rs863224476
23andMe	rs863224476
SNPshot	rs863224476
SNPdbe	rs863224476
MSV3d	rs863224476
GWAS Ctlg	rs863224476

Max Magnitude

6

ClinVar
Risk	rs863224476(-;-)
Alt	rs863224476(-;-)
Reference	Rs863224476(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030821delA
CLNSRC
CLNACC	RCV000196323.1,