rs1800935

Orientation

plus

Stabilized

plus

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

Make rs1800935(C;C)

Make rs1800935(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47795976

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1800935
dbSNP (classic)	rs1800935
ClinGen	rs1800935
ebi	rs1800935
HLI	rs1800935
Exac	rs1800935
Gnomad	rs1800935
Varsome	rs1800935
LitVar	rs1800935
Map	rs1800935
PheGenI	rs1800935
Biobank	rs1800935
1000 genomes	rs1800935
hgdp	rs1800935
ensembl	rs1800935
geneview	rs1800935
scholar	rs1800935
google	rs1800935
pharmgkb	rs1800935
gwascentral	rs1800935
openSNP	rs1800935
23andMe	rs1800935
SNPshot	rs1800935
SNPdbe	rs1800935
MSV3d	rs1800935
GWAS Ctlg	rs1800935

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

[PMID 24755277] Variations in mismatch repair genes and colorectal cancer risk and clinical outcome

ClinVar
Risk	rs1800935(C;C)
Alt	rs1800935(C;C)
Reference	Rs1800935(T;T)
Significance	Non-pathogenic
Disease	Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not specified Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48023115T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000030275.4, RCV000035326.8, RCV000131276.2,