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rs199754807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199754807(C;G)
Make rs199754807(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position60945369
GeneERCC8, NDUFAF2
is asnp
is mentioned by
dbSNPrs199754807
dbSNP (old)rs199754807
ClinGenrs199754807
ebirs199754807
HLIrs199754807
Exacrs199754807
Gnomadrs199754807
Varsomers199754807
Maprs199754807
PheGenIrs199754807
Biobankrs199754807
1000 genomesrs199754807
hgdprs199754807
ensemblrs199754807
gopubmedrs199754807
geneviewrs199754807
scholarrs199754807
googlers199754807
pharmgkbrs199754807
gwascentralrs199754807
openSNPrs199754807
23andMers199754807
23andMe allrs199754807
SNPshotrs199754807
SNPdbers199754807
MSV3drs199754807
GWAS Ctlgrs199754807
Max Magnitude0
ClinVar
Risk rs199754807(G;G)
Alt rs199754807(G;G)
Reference Rs199754807(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFAF2 ERCC8
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.60241196C>G
CLNSRC
CLNACC RCV000485122.1,