rs121908439

Orientation

minus

Stabilized

minus

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

Make rs121908439(C;C)

Make rs121908439(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

75032069

Gene

MLH3

is a	snp
is	mentioned by
dbSNP	rs121908439
dbSNP (classic)	rs121908439
ClinGen	rs121908439
ebi	rs121908439
HLI	rs121908439
Exac	rs121908439
Gnomad	rs121908439
Varsome	rs121908439
LitVar	rs121908439
Map	rs121908439
PheGenI	rs121908439
Biobank	rs121908439
1000 genomes	rs121908439
hgdp	rs121908439
ensembl	rs121908439
geneview	rs121908439
scholar	rs121908439
google	rs121908439
pharmgkb	rs121908439
gwascentral	rs121908439
openSNP	rs121908439
23andMe	rs121908439
SNPshot	rs121908439
SNPdbe	rs121908439
MSV3d	rs121908439
GWAS Ctlg	rs121908439

Max Magnitude

0

OMIM	604395
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121908439(C;C)
Alt	rs121908439(C;C)
Reference	Rs121908439(T;T)
Significance	Pathogenic
Disease	Hereditary nonpolyposis colorectal cancer type 7
Variation	info
Gene	MLH3
CLNDBN	Hereditary nonpolyposis colorectal cancer type 7
Reversed	1
HGVS	NC_000014.8:g.75498772A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005905.2,