rs108621

Orientation

plus

Stabilized

plus

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

Make rs108621(C;C)

Make rs108621(C;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

75013934

Gene

MLH3

is a	snp
is	mentioned by
dbSNP	rs108621
dbSNP (classic)	rs108621
ClinGen	rs108621
ebi	rs108621
HLI	rs108621
Exac	rs108621
Gnomad	rs108621
Varsome	rs108621
LitVar	rs108621
Map	rs108621
PheGenI	rs108621
Biobank	rs108621
1000 genomes	rs108621
hgdp	rs108621
ensembl	rs108621
geneview	rs108621
scholar	rs108621
google	rs108621
pharmgkb	rs108621
gwascentral	rs108621
openSNP	rs108621
23andMe	rs108621
SNPshot	rs108621
SNPdbe	rs108621
MSV3d	rs108621
GWAS Ctlg	rs108621

Max Magnitude

0

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

[PMID 24755277] Variations in mismatch repair genes and colorectal cancer risk and clinical outcome

ClinVar
Risk	rs108621(C;C)
Alt	rs108621(C;C)
Reference	Rs108621(T;T)
Significance	Probable-non-pathogenic
Disease	Lynch syndrome Leukoencephalopathy with vanishing white matter
Variation	info
Gene	MLH3
CLNDBN	Lynch syndrome Leukoencephalopathy with vanishing white matter
Reversed	0
HGVS	NC_000014.8:g.75480637T>C
CLNSRC
CLNACC	RCV000287442.1, RCV000356812.1,