rs28939071

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs28939071(A;A)

Make rs28939071(A;G)

Reference

GRCh38 38.1/142

Chromosome

14

Position

75017093

Gene

MLH3

is a	snp
is	mentioned by
dbSNP	rs28939071
dbSNP (classic)	rs28939071
ClinGen	rs28939071
ebi	rs28939071
HLI	rs28939071
Exac	rs28939071
Gnomad	rs28939071
Varsome	rs28939071
LitVar	rs28939071
Map	rs28939071
PheGenI	rs28939071
Biobank	rs28939071
1000 genomes	rs28939071
hgdp	rs28939071
ensembl	rs28939071
geneview	rs28939071
scholar	rs28939071
google	rs28939071
pharmgkb	rs28939071
gwascentral	rs28939071
openSNP	rs28939071
23andMe	rs28939071
SNPshot	rs28939071
SNPdbe	rs28939071
MSV3d	rs28939071
GWAS Ctlg	rs28939071

Max Magnitude

0

OMIM	604395
Desc	COLON CANCER, HEREDITARY NONPOLYPOSIS, TYPE 7
Variant	0005
Related	also

ClinVar
Risk	rs28939071(A;A)
Alt	rs28939071(A;A)
Reference	Rs28939071(G;G)
Significance	Non-pathogenic
Disease	Hereditary nonpolyposis colorectal cancer type 7 MLH3-Related Lynch Syndrome
Variation	info
Gene	MLH3
CLNDBN	Hereditary nonpolyposis colorectal cancer type 7 MLH3-Related Lynch Syndrome
Reversed	1
HGVS	NC_000014.8:g.75483796C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005902.2, RCV000232067.2,