rs1060502898

Orientation

plus

Stabilized

plus

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

Make rs1060502898(-;T)

Make rs1060502898(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47806858

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502898
dbSNP (classic)	rs1060502898
ClinGen	rs1060502898
ebi	rs1060502898
HLI	rs1060502898
Exac	rs1060502898
Gnomad	rs1060502898
Varsome	rs1060502898
LitVar	rs1060502898
Map	rs1060502898
PheGenI	rs1060502898
Biobank	rs1060502898
1000 genomes	rs1060502898
hgdp	rs1060502898
ensembl	rs1060502898
geneview	rs1060502898
scholar	rs1060502898
google	rs1060502898
pharmgkb	rs1060502898
gwascentral	rs1060502898
openSNP	rs1060502898
23andMe	rs1060502898
SNPshot	rs1060502898
SNPdbe	rs1060502898
MSV3d	rs1060502898
GWAS Ctlg	rs1060502898

Max Magnitude

0

ClinVar
Risk	rs1060502898(T;T) rs1060502898(TAT;TAT)
Alt	rs1060502898(T;T) rs1060502898(TAT;TAT)
Reference	Rs1060502898(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033969_48033997dup
CLNSRC
CLNACC	RCV000491731.1,