rs730881827

Orientation

plus

Stabilized

plus

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

Make rs730881827(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800815

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs730881827
dbSNP (classic)	rs730881827
ClinGen	rs730881827
ebi	rs730881827
HLI	rs730881827
Exac	rs730881827
Gnomad	rs730881827
Varsome	rs730881827
LitVar	rs730881827
Map	rs730881827
PheGenI	rs730881827
Biobank	rs730881827
1000 genomes	rs730881827
hgdp	rs730881827
ensembl	rs730881827
geneview	rs730881827
scholar	rs730881827
google	rs730881827
pharmgkb	rs730881827
gwascentral	rs730881827
openSNP	rs730881827
23andMe	rs730881827
SNPshot	rs730881827
SNPdbe	rs730881827
MSV3d	rs730881827
GWAS Ctlg	rs730881827

Max Magnitude

6

ClinVar
Risk	rs730881827(-;-)
Alt	rs730881827(-;-)
Reference	Rs730881827(AA;AA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome not provided Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027954_48027955delAA
CLNSRC
CLNACC	RCV000160743.2, RCV000254666.1, RCV000464722.1,