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rs774923951

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs774923951(C;C)
Make rs774923951(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position87589957
GeneORC3, RARS2
is asnp
is mentioned by
dbSNPrs774923951
ebirs774923951
HLIrs774923951
Exacrs774923951
Varsomers774923951
Maprs774923951
PheGenIrs774923951
hapmaprs774923951
1000 genomesrs774923951
hgdprs774923951
ensemblrs774923951
gopubmedrs774923951
geneviewrs774923951
scholarrs774923951
googlers774923951
pharmgkbrs774923951
gwascentralrs774923951
openSNPrs774923951
23andMers774923951
23andMe allrs774923951
SNP Nexus

SNPshotrs774923951
SNPdbers774923951
MSV3drs774923951
GWAS Ctlgrs774923951
Max Magnitude0
ClinVar
Risk rs774923951(A,C,G;A,C,G)
Alt rs774923951(A,C,G;A,C,G)
Reference rs774923951(T;T)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RARS2 ORC3
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000006.11:g.88299675T>C
CLNSRC
CLNACC RCV000210553.1,