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rs41297579

From SNPedia

Orientationminus
Stabilizedminus
Make rs41297579(A;A)
Make rs41297579(A;G)
Make rs41297579(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position157059397
GeneHAVCR1
is asnp
is mentioned by
dbSNPrs41297579
dbSNP (classic)rs41297579
ClinGenrs41297579
ebirs41297579
HLIrs41297579
Exacrs41297579
Gnomadrs41297579
Varsomers41297579
LitVarrs41297579
Maprs41297579
PheGenIrs41297579
Biobankrs41297579
1000 genomesrs41297579
hgdprs41297579
ensemblrs41297579
geneviewrs41297579
scholarrs41297579
googlers41297579
pharmgkbrs41297579
gwascentralrs41297579
openSNPrs41297579
23andMers41297579
SNPshotrs41297579
SNPdbers41297579
MSV3drs41297579
GWAS Ctlgrs41297579
GMAF0.1561
Max Magnitude0

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]


OMIM611162
DescMALARIA, SUSCEPTIBILITY TO
Variant
Relatedalso
OMIM606518
DescHEPATITIS A VIRUS CELLULAR RECEPTOR 1; HAVCR1
Variant
Relatedalso

[PMID 20070602] Fine mapping of T-cell immunoglobulin mucin domain gene 1 failed to detect a significant association with multiple sclerosis