rs876661251

Orientation

plus

Stabilized

plus

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

Make rs876661251(-;-)

Make rs876661251(-;CAGAACTTTGATCT)

Make rs876661251(CAGAACTTTGATCT;CAGAACTTTGATCT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799238

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876661251
dbSNP (classic)	rs876661251
ClinGen	rs876661251
ebi	rs876661251
HLI	rs876661251
Exac	rs876661251
Gnomad	rs876661251
Varsome	rs876661251
LitVar	rs876661251
Map	rs876661251
PheGenI	rs876661251
Biobank	rs876661251
1000 genomes	rs876661251
hgdp	rs876661251
ensembl	rs876661251
geneview	rs876661251
scholar	rs876661251
google	rs876661251
pharmgkb	rs876661251
gwascentral	rs876661251
openSNP	rs876661251
23andMe	rs876661251
SNPshot	rs876661251
SNPdbe	rs876661251
MSV3d	rs876661251
GWAS Ctlg	rs876661251

Max Magnitude

0

ClinVar
Risk	rs876661251(-;-)
Alt	rs876661251(-;-)
Reference	Rs876661251(TCTCAGAACTTTGA;TCTCAGAACTTTGA)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MSH6
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.48026377_48026390delCAGAACTTTGATCT
CLNSRC
CLNACC	RCV000217315.1,