rs863225411

Orientation

plus

Stabilized

plus

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

Make rs863225411(-;AGAA)

Make rs863225411(AGAA;AGAA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47806259

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs863225411
dbSNP (classic)	rs863225411
ClinGen	rs863225411
ebi	rs863225411
HLI	rs863225411
Exac	rs863225411
Gnomad	rs863225411
Varsome	rs863225411
LitVar	rs863225411
Map	rs863225411
PheGenI	rs863225411
Biobank	rs863225411
1000 genomes	rs863225411
hgdp	rs863225411
ensembl	rs863225411
geneview	rs863225411
scholar	rs863225411
google	rs863225411
pharmgkb	rs863225411
gwascentral	rs863225411
openSNP	rs863225411
23andMe	rs863225411
SNPshot	rs863225411
SNPdbe	rs863225411
MSV3d	rs863225411
GWAS Ctlg	rs863225411

Max Magnitude

0

ClinVar
Risk	rs863225411(AAGAA;AAGAA) rs863225411(AGAA;AGAA)
Alt	rs863225411(AAGAA;AAGAA) rs863225411(AGAA;AGAA)
Reference	Rs863225411(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48033394_48033398dup; NC_000002.11:g.48033395_48033398dupAGAA
CLNSRC
CLNACC	RCV000491792.1, RCV000202173.1, RCV000491958.1,