rs878853736

Orientation

plus

Stabilized

plus

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

Make rs878853736(-;AAAAT)

Make rs878853736(AAAAT;AAAAT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806278

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs878853736
dbSNP (classic)	rs878853736
ClinGen	rs878853736
ebi	rs878853736
HLI	rs878853736
Exac	rs878853736
Gnomad	rs878853736
Varsome	rs878853736
LitVar	rs878853736
Map	rs878853736
PheGenI	rs878853736
Biobank	rs878853736
1000 genomes	rs878853736
hgdp	rs878853736
ensembl	rs878853736
geneview	rs878853736
scholar	rs878853736
google	rs878853736
pharmgkb	rs878853736
gwascentral	rs878853736
openSNP	rs878853736
23andMe	rs878853736
SNPshot	rs878853736
SNPdbe	rs878853736
MSV3d	rs878853736
GWAS Ctlg	rs878853736

Max Magnitude

0

ClinVar
Risk	rs878853736(ATAAA;ATAAA)
Alt	rs878853736(ATAAA;ATAAA)
Reference	Rs878853736(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033413_48033417dupAAAAT
CLNSRC
CLNACC	RCV000232271.1,