rs63750448

Orientation

plus

Stabilized

plus

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

Make rs63750448(A;C)

Make rs63750448(C;C)

Reference

GRCh38 38.1/142

Chromosome

17

Position

44351792

Gene

GRN

is a	snp
is	mentioned by
dbSNP	rs63750448
dbSNP (classic)	rs63750448
ClinGen	rs63750448
ebi	rs63750448
HLI	rs63750448
Exac	rs63750448
Gnomad	rs63750448
Varsome	rs63750448
LitVar	rs63750448
Map	rs63750448
PheGenI	rs63750448
Biobank	rs63750448
1000 genomes	rs63750448
hgdp	rs63750448
ensembl	rs63750448
geneview	rs63750448
scholar	rs63750448
google	rs63750448
pharmgkb	rs63750448
gwascentral	rs63750448
openSNP	rs63750448
23andMe	rs63750448
SNPshot	rs63750448
SNPdbe	rs63750448
MSV3d	rs63750448
GWAS Ctlg	rs63750448

Max Magnitude

0

[PMID 25986311] Association between MutL homolog 1 polymorphisms and the risk of colorectal cancer: a meta-analysis

ClinVar
Risk	rs63750448(C;C)
Alt	rs63750448(C;C)
Reference	Rs63750448(A;A)
Significance	Untested
Disease	not provided
Variation	info
Gene	GRN
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.42429160A>C
CLNSRC
CLNACC	RCV000084475.1,