rs730881830

Orientation

plus

Stabilized

plus

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

Make rs730881830(-;TC)

Make rs730881830(TC;TC)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47806590

Gene	FBXO11, MSH6

is a	snp
is	mentioned by
dbSNP	rs730881830
dbSNP (classic)	rs730881830
ClinGen	rs730881830
ebi	rs730881830
HLI	rs730881830
Exac	rs730881830
Gnomad	rs730881830
Varsome	rs730881830
LitVar	rs730881830
Map	rs730881830
PheGenI	rs730881830
Biobank	rs730881830
1000 genomes	rs730881830
hgdp	rs730881830
ensembl	rs730881830
geneview	rs730881830
scholar	rs730881830
google	rs730881830
pharmgkb	rs730881830
gwascentral	rs730881830
openSNP	rs730881830
23andMe	rs730881830
SNPshot	rs730881830
SNPdbe	rs730881830
MSV3d	rs730881830
GWAS Ctlg	rs730881830

Max Magnitude

0

ClinVar
Risk	rs730881830(TC;TC)
Alt	rs730881830(TC;TC)
Reference	Rs730881830(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	FBXO11 MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48033728_48033729dupTC
CLNSRC
CLNACC	RCV000160746.2,