rs876658864

Orientation

plus

Stabilized

plus

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

Make rs876658864(GG;GG)

Make rs876658864(GG;TGGCCCT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47800019

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876658864
dbSNP (classic)	rs876658864
ClinGen	rs876658864
ebi	rs876658864
HLI	rs876658864
Exac	rs876658864
Gnomad	rs876658864
Varsome	rs876658864
LitVar	rs876658864
Map	rs876658864
PheGenI	rs876658864
Biobank	rs876658864
1000 genomes	rs876658864
hgdp	rs876658864
ensembl	rs876658864
geneview	rs876658864
scholar	rs876658864
google	rs876658864
pharmgkb	rs876658864
gwascentral	rs876658864
openSNP	rs876658864
23andMe	rs876658864
SNPshot	rs876658864
SNPdbe	rs876658864
MSV3d	rs876658864
GWAS Ctlg	rs876658864

Max Magnitude

0

ClinVar
Risk	rs876658864(GG;GG)
Alt	rs876658864(GG;GG)
Reference	Rs876658864(TGGCCCT;TGGCCCT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027158_48027164delTGGCCCTinsGG
CLNSRC
CLNACC	RCV000219907.1,