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rs2045065

From SNPedia

Orientationminus
Stabilizedminus
Make rs2045065(C;C)
Make rs2045065(C;T)
Make rs2045065(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position1058700
GeneRNF212
is asnp
is mentioned by
dbSNPrs2045065
ebirs2045065
HLIrs2045065
Exacrs2045065
Varsomers2045065
Maprs2045065
PheGenIrs2045065
hapmaprs2045065
1000 genomesrs2045065
hgdprs2045065
ensemblrs2045065
gopubmedrs2045065
geneviewrs2045065
scholarrs2045065
googlers2045065
pharmgkbrs2045065
gwascentralrs2045065
openSNPrs2045065
23andMers2045065
23andMe allrs2045065
SNP Nexus

SNPshotrs2045065
SNPdbers2045065
MSV3drs2045065
GWAS Ctlgrs2045065
GMAF0.2282
Max Magnitude
? (C;C) (C;T) (T;T) 28
OMIM612042
DescRECOMBINATION RATE QUANTITATIVE TRAIT LOCUS 1; RRQTL1
Variant
Relatedalso



GET Evidence
rs2045065
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.84375
summary