rs1650697

minus

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

Make rs1650697(C;C)

Make rs1650697(C;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

80654962

Gene	DHFR, MSH3

is a	snp
is	mentioned by
dbSNP	rs1650697
dbSNP (classic)	rs1650697
ClinGen	rs1650697
ebi	rs1650697
HLI	rs1650697
Exac	rs1650697
Gnomad	rs1650697
Varsome	rs1650697
LitVar	rs1650697
Map	rs1650697
PheGenI	rs1650697
Biobank	rs1650697
1000 genomes	rs1650697
hgdp	rs1650697
ensembl	rs1650697
geneview	rs1650697
scholar	rs1650697
google	rs1650697
pharmgkb	rs1650697
gwascentral	rs1650697
openSNP	rs1650697
23andMe	rs1650697
SNPshot	rs1650697
SNPdbe	rs1650697
MSV3d	rs1650697
GWAS Ctlg	rs1650697

GMAF

0.2268

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 20737570] Genetic variants in one-carbon metabolism-related genes contribute to NSCLC prognosis in a Chinese population

[PMID 18551366 ] Genetic variation in DNA repair pathway genes and premenopausal breast cancer risk.

[PMID 19493349 ] 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

[PMID 20472929] Folate pathway enzyme gene polymorphisms and the efficacy and toxicity of methotrexate in psoriatic arthritis.

[PMID 25759212 ] A distinct and replicable variant of the squamous cell carcinoma gene inositol polyphosphate-5-phosphatase modifies the susceptibility of arsenic-associated skin lesions in Bangladesh

[PMID 24732178] Pharmacogenetics of pemetrexed combination therapy in lung cancer: pathway analysis reveals novel toxicity associations

ClinVar
Risk	rs1650697(C;C)
Alt	rs1650697(C;C)
Reference	Rs1650697(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	DHFR MSH3
CLNDBN	not specified
Reversed	1
HGVS	NC_000005.9:g.79950781A>G
CLNSRC
CLNACC	RCV000454914.1,