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rs875989813

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs875989813(-;-)
Make rs875989813(-;T)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position45159081
GeneFANCM
is asnp
is mentioned by
dbSNPrs875989813
ebirs875989813
HLIrs875989813
Exacrs875989813
Varsomers875989813
Maprs875989813
PheGenIrs875989813
hapmaprs875989813
1000 genomesrs875989813
hgdprs875989813
ensemblrs875989813
gopubmedrs875989813
geneviewrs875989813
scholarrs875989813
googlers875989813
pharmgkbrs875989813
gwascentralrs875989813
openSNPrs875989813
23andMers875989813
23andMe allrs875989813
SNP Nexus

SNPshotrs875989813
SNPdbers875989813
MSV3drs875989813
GWAS Ctlgrs875989813
Max Magnitude0
ClinVar
Risk rs875989813(;)
Alt rs875989813(;)
Reference rs875989813(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCM
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.45628284delT
CLNSRC
CLNACC RCV000171476.1,