Have questions? Visit https://www.reddit.com/r/SNPedia

rs786204005

From SNPedia

Orientationminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786204005(-;-)
Make rs786204005(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position11803156
GeneMTHFR
is asnp
is mentioned by
dbSNPrs786204005
ebirs786204005
HLIrs786204005
Exacrs786204005
Varsomers786204005
Maprs786204005
PheGenIrs786204005
hapmaprs786204005
1000 genomesrs786204005
hgdprs786204005
ensemblrs786204005
gopubmedrs786204005
geneviewrs786204005
scholarrs786204005
googlers786204005
pharmgkbrs786204005
gwascentralrs786204005
openSNPrs786204005
23andMers786204005
23andMe allrs786204005
SNP Nexus

SNPshotrs786204005
SNPdbers786204005
MSV3drs786204005
GWAS Ctlgrs786204005
Max Magnitude0
ClinVar
Risk rs786204005(;)
Alt rs786204005(;)
Reference rs786204005(CT;CT)
Significance Pathogenic
Disease Homocysteinemia due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocysteinemia due to MTHFR deficiency
Reversed 1
HGVS NC_000001.10:g.11863213_11863214delAG
CLNSRC
CLNACC RCV000167585.1,