rs876659189

Orientation

plus

Stabilized

plus

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

Make rs876659189(-;TT)

Make rs876659189(TT;TT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47800788

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876659189
dbSNP (classic)	rs876659189
ClinGen	rs876659189
ebi	rs876659189
HLI	rs876659189
Exac	rs876659189
Gnomad	rs876659189
Varsome	rs876659189
LitVar	rs876659189
Map	rs876659189
PheGenI	rs876659189
Biobank	rs876659189
1000 genomes	rs876659189
hgdp	rs876659189
ensembl	rs876659189
geneview	rs876659189
scholar	rs876659189
google	rs876659189
pharmgkb	rs876659189
gwascentral	rs876659189
openSNP	rs876659189
23andMe	rs876659189
SNPshot	rs876659189
SNPdbe	rs876659189
MSV3d	rs876659189
GWAS Ctlg	rs876659189

Max Magnitude

0

ClinVar
Risk	rs876659189(TT;TT)
Alt	rs876659189(TT;TT)
Reference	Rs876659189(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027927_48027928insTT
CLNSRC
CLNACC	RCV000218854.1,