rs541941351
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common/normal |
Make rs541941351(A;A) |
Make rs541941351(A;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 2 |
Position | 24918797 |
Gene | ADCY3 |
is a | snp |
is | mentioned by |
dbSNP | rs541941351 |
dbSNP (classic) | rs541941351 |
ClinGen | rs541941351 |
ebi | rs541941351 |
HLI | rs541941351 |
Exac | rs541941351 |
Gnomad | rs541941351 |
Varsome | rs541941351 |
LitVar | rs541941351 |
Map | rs541941351 |
PheGenI | rs541941351 |
Biobank | rs541941351 |
1000 genomes | rs541941351 |
hgdp | rs541941351 |
ensembl | rs541941351 |
geneview | rs541941351 |
scholar | rs541941351 |
rs541941351 | |
pharmgkb | rs541941351 |
gwascentral | rs541941351 |
openSNP | rs541941351 |
23andMe | rs541941351 |
SNPshot | rs541941351 |
SNPdbe | rs541941351 |
MSV3d | rs541941351 |
GWAS Ctlg | rs541941351 |
Max Magnitude | 0 |
rs541941351, also known as c.191A>T or p.Asn64Ile, represents a rare variant in the ADCY3 gene. It has been reported as potentially causing obesity when inherited recessively, but heterozygotes may be affected to a lesser degree, if this variant is driving related GWAS findings.[PMID 29311637]
Be aware of orientation & ambiguous flip issues due to the A/T nature of this variant and the reverse orientation of the gene.