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rs186476170

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs186476170(G;T)
Make rs186476170(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161213712
GeneFCER1G, NDUFS2
is asnp
is mentioned by
dbSNPrs186476170
ebirs186476170
HLIrs186476170
Exacrs186476170
Varsomers186476170
Maprs186476170
PheGenIrs186476170
hapmaprs186476170
1000 genomesrs186476170
hgdprs186476170
ensemblrs186476170
gopubmedrs186476170
geneviewrs186476170
scholarrs186476170
googlers186476170
pharmgkbrs186476170
gwascentralrs186476170
openSNPrs186476170
23andMers186476170
23andMe allrs186476170
SNP Nexus

SNPshotrs186476170
SNPdbers186476170
MSV3drs186476170
GWAS Ctlgrs186476170
Max Magnitude0
ClinVar
Risk rs186476170(T;T)
Alt rs186476170(T;T)
Reference rs186476170(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFS2 FCER1G
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161183502G>T
CLNSRC
CLNACC RCV000199918.1,