rs41297577
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs41297577(C;C) |
Make rs41297577(C;G) |
Make rs41297577(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 157059492 |
Gene | HAVCR1 |
is a | snp |
is | mentioned by |
dbSNP | rs41297577 |
dbSNP (classic) | rs41297577 |
ClinGen | rs41297577 |
ebi | rs41297577 |
HLI | rs41297577 |
Exac | rs41297577 |
Gnomad | rs41297577 |
Varsome | rs41297577 |
LitVar | rs41297577 |
Map | rs41297577 |
PheGenI | rs41297577 |
Biobank | rs41297577 |
1000 genomes | rs41297577 |
hgdp | rs41297577 |
ensembl | rs41297577 |
geneview | rs41297577 |
scholar | rs41297577 |
rs41297577 | |
pharmgkb | rs41297577 |
gwascentral | rs41297577 |
openSNP | rs41297577 |
23andMe | rs41297577 |
SNPshot | rs41297577 |
SNPdbe | rs41297577 |
MSV3d | rs41297577 |
GWAS Ctlg | rs41297577 |
GMAF | 0.2608 |
Max Magnitude | 0 |
A study of 78 adult Thai patients infected with P. falciparum malaria reported that the TIM1 promoter haplotype comprising three derived alleles, -1637A rs7702919, -1549C rs41297577 and -1454A rs41297579, which were in complete linkage disequilibrium, was significantly associated with protection against cerebral malaria, a major life-threatening complication (OR = 0.41; CI: 0.24-0.71; P= 0.0009).[PMID 18294362]
[PMID 20070602] Fine mapping of T-cell immunoglobulin mucin domain gene 1 failed to detect a significant association with multiple sclerosis