rs587782277

Orientation

plus

Stabilized

plus

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

Make rs587782277(-;A)

Make rs587782277(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800762

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782277
dbSNP (classic)	rs587782277
ClinGen	rs587782277
ebi	rs587782277
HLI	rs587782277
Exac	rs587782277
Gnomad	rs587782277
Varsome	rs587782277
LitVar	rs587782277
Map	rs587782277
PheGenI	rs587782277
Biobank	rs587782277
1000 genomes	rs587782277
hgdp	rs587782277
ensembl	rs587782277
geneview	rs587782277
scholar	rs587782277
google	rs587782277
pharmgkb	rs587782277
gwascentral	rs587782277
openSNP	rs587782277
23andMe	rs587782277
SNPshot	rs587782277
SNPdbe	rs587782277
MSV3d	rs587782277
GWAS Ctlg	rs587782277

Merged from

Rs763978082

Max Magnitude

0

ClinVar
Risk	rs587782277(A;A)
Alt	rs587782277(A;A)
Reference	Rs587782277(-;-)
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.48027901dupA
CLNSRC
CLNACC	RCV000131134.2, RCV000218611.2,