rs863225399

Orientation

plus

Stabilized

plus

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

Make rs863225399(-;A)

Make rs863225399(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47799295

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs863225399
dbSNP (classic)	rs863225399
ClinGen	rs863225399
ebi	rs863225399
HLI	rs863225399
Exac	rs863225399
Gnomad	rs863225399
Varsome	rs863225399
LitVar	rs863225399
Map	rs863225399
PheGenI	rs863225399
Biobank	rs863225399
1000 genomes	rs863225399
hgdp	rs863225399
ensembl	rs863225399
geneview	rs863225399
scholar	rs863225399
google	rs863225399
pharmgkb	rs863225399
gwascentral	rs863225399
openSNP	rs863225399
23andMe	rs863225399
SNPshot	rs863225399
SNPdbe	rs863225399
MSV3d	rs863225399
GWAS Ctlg	rs863225399

Max Magnitude

0

ClinVar
Risk	rs863225399(A;A)
Alt	rs863225399(A;A)
Reference	Rs863225399(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH6
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.48026434dupA
CLNSRC
CLNACC	RCV000202043.1,