rs175080

plus

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

Make rs175080(A;A)

Make rs175080(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

14

Position

75047125

Gene

MLH3

is a	snp
is	mentioned by
dbSNP	rs175080
dbSNP (classic)	rs175080
ClinGen	rs175080
ebi	rs175080
HLI	rs175080
Exac	rs175080
Gnomad	rs175080
Varsome	rs175080
LitVar	rs175080
Map	rs175080
PheGenI	rs175080
Biobank	rs175080
1000 genomes	rs175080
hgdp	rs175080
ensembl	rs175080
geneview	rs175080
scholar	rs175080
google	rs175080
pharmgkb	rs175080
gwascentral	rs175080
openSNP	rs175080
23andMe	rs175080
SNPshot	rs175080
SNPdbe	rs175080
MSV3d	rs175080
GWAS Ctlg	rs175080

Max Magnitude

0

?

(A;A) (A;G) (G;G)

28

[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	rs175080(A;A)
Alt	rs175080(A;A)
Reference	Rs175080(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Lynch syndrome
Variation	info
Gene	MLH3
CLNDBN	not specified Lynch syndrome
Reversed	0
HGVS	NC_000014.8:g.75513828G>A
CLNSRC
CLNACC	RCV000253289.1, RCV000385582.1,

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