rs763978082

Merged into

rs587782277

Orientation

plus

Stabilized

plus

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

Make rs763978082(-;A)

Make rs763978082(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800761

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs763978082
dbSNP (classic)	rs763978082
ClinGen	rs763978082
ebi	rs763978082
HLI	rs763978082
Exac	rs763978082
Gnomad	rs763978082
Varsome	rs763978082
LitVar	rs763978082
Map	rs763978082
PheGenI	rs763978082
Biobank	rs763978082
1000 genomes	rs763978082
hgdp	rs763978082
ensembl	rs763978082
geneview	rs763978082
scholar	rs763978082
google	rs763978082
pharmgkb	rs763978082
gwascentral	rs763978082
openSNP	rs763978082
23andMe	rs763978082
SNPshot	rs763978082
SNPdbe	rs763978082
MSV3d	rs763978082
GWAS Ctlg	rs763978082

Status

Merged into rs587782277

Max Magnitude

0

ClinVar
Risk	rs763978082(A;A)
Alt	rs763978082(A;A)
Reference	Rs763978082(;)
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, RCV000218611.1,