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

rs201408725

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201408725(C;T)
Make rs201408725(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position158690264
GeneGFM1
is asnp
is mentioned by
dbSNPrs201408725
ebirs201408725
HLIrs201408725
Exacrs201408725
Varsomers201408725
Maprs201408725
PheGenIrs201408725
hapmaprs201408725
1000 genomesrs201408725
hgdprs201408725
ensemblrs201408725
gopubmedrs201408725
geneviewrs201408725
scholarrs201408725
googlers201408725
pharmgkbrs201408725
gwascentralrs201408725
openSNPrs201408725
23andMers201408725
23andMe allrs201408725
SNP Nexus

SNPshotrs201408725
SNPdbers201408725
MSV3drs201408725
GWAS Ctlgrs201408725
Max Magnitude0
ClinVar
Risk rs201408725(T;T)
Alt rs201408725(T;T)
Reference rs201408725(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GFM1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.158408053C>T
CLNSRC
CLNACC RCV000197077.2,