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rs41297577

From SNPedia

Orientationminus
Stabilizedminus
Make rs41297577(C;C)
Make rs41297577(C;G)
Make rs41297577(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position157059492
GeneHAVCR1
is asnp
is mentioned by
dbSNPrs41297577
dbSNP (classic)rs41297577
ClinGenrs41297577
ebirs41297577
HLIrs41297577
Exacrs41297577
Gnomadrs41297577
Varsomers41297577
LitVarrs41297577
Maprs41297577
PheGenIrs41297577
Biobankrs41297577
1000 genomesrs41297577
hgdprs41297577
ensemblrs41297577
geneviewrs41297577
scholarrs41297577
googlers41297577
pharmgkbrs41297577
gwascentralrs41297577
openSNPrs41297577
23andMers41297577
SNPshotrs41297577
SNPdbers41297577
MSV3drs41297577
GWAS Ctlgrs41297577
GMAF0.2608
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