rs1060502937

Orientation

plus

Stabilized

plus

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

Make rs1060502937(A;T)

Make rs1060502937(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47806623

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502937
dbSNP (classic)	rs1060502937
ClinGen	rs1060502937
ebi	rs1060502937
HLI	rs1060502937
Exac	rs1060502937
Gnomad	rs1060502937
Varsome	rs1060502937
LitVar	rs1060502937
Map	rs1060502937
PheGenI	rs1060502937
Biobank	rs1060502937
1000 genomes	rs1060502937
hgdp	rs1060502937
ensembl	rs1060502937
geneview	rs1060502937
scholar	rs1060502937
google	rs1060502937
pharmgkb	rs1060502937
gwascentral	rs1060502937
openSNP	rs1060502937
23andMe	rs1060502937
SNPshot	rs1060502937
SNPdbe	rs1060502937
MSV3d	rs1060502937
GWAS Ctlg	rs1060502937

Max Magnitude

0

ClinVar
Risk	rs1060502937(T;T)
Alt	rs1060502937(T;T)
Reference	Rs1060502937(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48033762A>T
CLNSRC
CLNACC	RCV000467214.1,