rs863224474

Orientation

plus

Stabilized

plus

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

Make rs863224474(-;T)

Make rs863224474(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47799727

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs863224474
dbSNP (classic)	rs863224474
ClinGen	rs863224474
ebi	rs863224474
HLI	rs863224474
Exac	rs863224474
Gnomad	rs863224474
Varsome	rs863224474
LitVar	rs863224474
Map	rs863224474
PheGenI	rs863224474
Biobank	rs863224474
1000 genomes	rs863224474
hgdp	rs863224474
ensembl	rs863224474
geneview	rs863224474
scholar	rs863224474
google	rs863224474
pharmgkb	rs863224474
gwascentral	rs863224474
openSNP	rs863224474
23andMe	rs863224474
SNPshot	rs863224474
SNPdbe	rs863224474
MSV3d	rs863224474
GWAS Ctlg	rs863224474

Max Magnitude

0

ClinVar
Risk	rs863224474(T;T)
Alt	rs863224474(T;T)
Reference	Rs863224474(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026866dupT
CLNSRC
CLNACC	RCV000195900.1,