rs1042821

minus

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

Make rs1042821(C;T)

Make rs1042821(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47783349

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1042821
dbSNP (classic)	rs1042821
ClinGen	rs1042821
ebi	rs1042821
HLI	rs1042821
Exac	rs1042821
Gnomad	rs1042821
Varsome	rs1042821
LitVar	rs1042821
Map	rs1042821
PheGenI	rs1042821
Biobank	rs1042821
1000 genomes	rs1042821
hgdp	rs1042821
ensembl	rs1042821
geneview	rs1042821
scholar	rs1042821
google	rs1042821
pharmgkb	rs1042821
gwascentral	rs1042821
openSNP	rs1042821
23andMe	rs1042821
SNPshot	rs1042821
SNPdbe	rs1042821
MSV3d	rs1042821
GWAS Ctlg	rs1042821

Max Magnitude

0

[PMID 26027715] Correlation between polymorphisms in DNA mismatch repair genes and the risk of primary hepatocellular carcinoma for the Han population in northern China

ClinVar
Risk	rs1042821(G;G) rs1042821(T;T)
Alt	rs1042821(G;G) rs1042821(T;T)
Reference	Rs1042821(C;C)
Significance	Non-pathogenic
Disease	Lynch syndrome not provided not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided not specified Hereditary cancer-predisposing syndrome Lynch syndrome I
Reversed	1
HGVS	NC_000002.11:g.48010488G>A; NC_000002.11:g.48010488G>C
CLNSRC	HGMD UniProtKB (protein)
CLNACC	RCV000030258.4, RCV000034489.1, RCV000035318.9, RCV000132091.3, RCV000144626.1, RCV000480607.1,

[PMID 29616133 ] Mismatch repair single nucleotide polymorphisms and thyroid cancer susceptibility.

[PMID 31374908 ] Thyroid Cancer: The Quest for Genetic Susceptibility Involving DNA Repair Genes.