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rs586178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs586178(C;C)
Make rs586178(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position25420739
GeneRHCE
is asnp
is mentioned by
dbSNPrs586178
ebirs586178
HLIrs586178
Exacrs586178
Varsomers586178
Maprs586178
PheGenIrs586178
hapmaprs586178
1000 genomesrs586178
hgdprs586178
ensemblrs586178
gopubmedrs586178
geneviewrs586178
scholarrs586178
googlers586178
pharmgkbrs586178
gwascentralrs586178
openSNPrs586178
23andMers586178
23andMe allrs586178
SNP Nexus

SNPshotrs586178
SNPdbers586178
MSV3drs586178
GWAS Ctlgrs586178
GMAF0.3421
Max Magnitude0
OMIM111700
Desc
Variant0002
Relatedalso


GET Evidence
RHCE-C16W
aa_change Cys16Trp
aa_change_short C16W
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.254685
summary



ClinVar
Risk rs586178(A,C;A,C)
Alt rs586178(A,C;A,C)
Reference rs586178(G;G)
Significance Non-pathogenic
Disease RH C/c POLYMORPHISM
Variation info
Gene RHCE
CLNDBN RH C/c POLYMORPHISM
Reversed 0
HGVS NC_000001.10:g.25747230G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019283.2,