rs175081

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(T;T)	0	common in clinvar

Make rs175081(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

75047180

Gene

MLH3

is a	snp
is	mentioned by
dbSNP	rs175081
dbSNP (classic)	rs175081
ClinGen	rs175081
ebi	rs175081
HLI	rs175081
Exac	rs175081
Gnomad	rs175081
Varsome	rs175081
LitVar	rs175081
Map	rs175081
PheGenI	rs175081
Biobank	rs175081
1000 genomes	rs175081
hgdp	rs175081
ensembl	rs175081
geneview	rs175081
scholar	rs175081
google	rs175081
pharmgkb	rs175081
gwascentral	rs175081
openSNP	rs175081
23andMe	rs175081
SNPshot	rs175081
SNPdbe	rs175081
MSV3d	rs175081
GWAS Ctlg	rs175081

GMAF

0.006887

Max Magnitude

0

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

ClinVar
Risk	Rs175081(C;C)
Alt	Rs175081(C;C)
Reference	Rs175081(T;T)
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.75513883T>C
CLNSRC
CLNACC	RCV000249947.1, RCV000293688.1,