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rs561425038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs561425038(C;C)
Make rs561425038(C;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position35119613
GeneFNDC8, RAD51D, RAD51L3-RFFL
is asnp
is mentioned by
dbSNPrs561425038
ebirs561425038
HLIrs561425038
Exacrs561425038
Varsomers561425038
Maprs561425038
PheGenIrs561425038
hapmaprs561425038
1000 genomesrs561425038
hgdprs561425038
ensemblrs561425038
gopubmedrs561425038
geneviewrs561425038
scholarrs561425038
googlers561425038
pharmgkbrs561425038
gwascentralrs561425038
openSNPrs561425038
23andMers561425038
23andMe allrs561425038
SNP Nexus

SNPshotrs561425038
SNPdbers561425038
MSV3drs561425038
GWAS Ctlgrs561425038
Max Magnitude0
ClinVar
Risk rs561425038(C;C)
Alt rs561425038(C;C)
Reference rs561425038(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RAD51D RAD51L3-RFFL FNDC8
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.33446632T>C
CLNSRC ClinVar GeneDx
CLNACC RCV000115810.3,