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rs768434408

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs768434408(A;G)
Make rs768434408(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position11790682
GeneMTHFR
is asnp
is mentioned by
dbSNPrs768434408
ebirs768434408
HLIrs768434408
Exacrs768434408
Varsomers768434408
Maprs768434408
PheGenIrs768434408
hapmaprs768434408
1000 genomesrs768434408
hgdprs768434408
ensemblrs768434408
gopubmedrs768434408
geneviewrs768434408
scholarrs768434408
googlers768434408
pharmgkbrs768434408
gwascentralrs768434408
openSNPrs768434408
23andMers768434408
23andMe allrs768434408
SNP Nexus

SNPshotrs768434408
SNPdbers768434408
MSV3drs768434408
GWAS Ctlgrs768434408
Max Magnitude0
ClinVar
Risk rs768434408(G;G)
Alt rs768434408(G;G)
Reference rs768434408(A;A)
Significance Pathogenic
Disease Homocysteinemia due to MTHFR deficiency
Variation info
Gene MTHFR
CLNDBN Homocysteinemia due to MTHFR deficiency
Reversed 0
HGVS NC_000001.10:g.11850739A>G
CLNSRC
CLNACC RCV000167626.1,