rs876658497

Orientation

plus

Stabilized

plus

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

Make rs876658497(-;AAGT)

Make rs876658497(AAGT;AAGT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806784

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs876658497
dbSNP (classic)	rs876658497
ClinGen	rs876658497
ebi	rs876658497
HLI	rs876658497
Exac	rs876658497
Gnomad	rs876658497
Varsome	rs876658497
LitVar	rs876658497
Map	rs876658497
PheGenI	rs876658497
Biobank	rs876658497
1000 genomes	rs876658497
hgdp	rs876658497
ensembl	rs876658497
geneview	rs876658497
scholar	rs876658497
google	rs876658497
pharmgkb	rs876658497
gwascentral	rs876658497
openSNP	rs876658497
23andMe	rs876658497
SNPshot	rs876658497
SNPdbe	rs876658497
MSV3d	rs876658497
GWAS Ctlg	rs876658497

Max Magnitude

0

ClinVar
Risk	rs876658497(AAGT;AAGT)
Alt	rs876658497(AAGT;AAGT)
Reference	Rs876658497(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033920_48033923dupAAGT
CLNSRC
CLNACC	RCV000219545.1,