rs61996318
From SNPedia
Orientation | plus |
Make rs61996318(G;G) |
Make rs61996318(G;T) |
Make rs61996318(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 2 |
Position | 48714023 |
Gene | LHCGR, STON1-GTF2A1L |
is a | snp |
is | mentioned by |
dbSNP | rs61996318 |
dbSNP (classic) | rs61996318 |
ClinGen | rs61996318 |
ebi | rs61996318 |
HLI | rs61996318 |
Exac | rs61996318 |
Gnomad | rs61996318 |
Varsome | rs61996318 |
LitVar | rs61996318 |
Map | rs61996318 |
PheGenI | rs61996318 |
Biobank | rs61996318 |
1000 genomes | rs61996318 |
hgdp | rs61996318 |
ensembl | rs61996318 |
geneview | rs61996318 |
scholar | rs61996318 |
rs61996318 | |
pharmgkb | rs61996318 |
gwascentral | rs61996318 |
openSNP | rs61996318 |
23andMe | rs61996318 |
SNPshot | rs61996318 |
SNPdbe | rs61996318 |
MSV3d | rs61996318 |
GWAS Ctlg | rs61996318 |
Max Magnitude | 0 |
[PMID 30958034] Association of Luteinizing hormone and LH receptor gene polymorphism with susceptibility of Polycystic ovary syndrome.