Rs119478058

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Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs119478058(C;T)
Make rs119478058(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position102923789
GeneAMN
is asnp
is mentioned by
dbSNPrs119478058
PheGenIrs119478058
nextbiors119478058
hapmaprs119478058
1000 genomesrs119478058
hgdprs119478058
ensemblrs119478058
gopubmedrs119478058
geneviewrs119478058
scholarrs119478058
googlers119478058
pharmgkbrs119478058
gwascentralrs119478058
openSNPrs119478058
23andMers119478058
23andMe allrs119478058
SNP Nexus

SNPshotrs119478058
SNPdbers119478058
MSV3drs119478058
Merged fromRs28939377
Max Magnitude0
OMIM605799
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119478058(T;T)
Alt rs119478058(T;T)
Reference rs119478058(C;C)
Significance Pathogenic
Disease Megaloblastic anemia 1
Variation info
Gene AMN
CLNDBN Megaloblastic anemia 1, Norwegian type
Reversed 0
HGVS NC_000014.8:g.103390126C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005036.1,