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rs797045116

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045116(-;A)
Make rs797045116(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position45159190
GeneFANCM
is asnp
is mentioned by
dbSNPrs797045116
dbSNP (old)rs797045116
ClinGenrs797045116
ebirs797045116
HLIrs797045116
Exacrs797045116
Gnomadrs797045116
Varsomers797045116
Maprs797045116
PheGenIrs797045116
Biobankrs797045116
1000 genomesrs797045116
hgdprs797045116
ensemblrs797045116
gopubmedrs797045116
geneviewrs797045116
scholarrs797045116
googlers797045116
pharmgkbrs797045116
gwascentralrs797045116
openSNPrs797045116
23andMers797045116
23andMe allrs797045116
SNP Nexus

SNPshotrs797045116
SNPdbers797045116
MSV3drs797045116
GWAS Ctlgrs797045116
Max Magnitude0
ClinVar
Risk rs797045116(A;A)
Alt rs797045116(A;A)
Reference Rs797045116(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FANCM
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.45628393dupA
CLNSRC
CLNACC RCV000190644.1,