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rs754367349

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs754367349(-;-)
Make rs754367349(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position58709927
GeneRAD51C
is asnp
is mentioned by
dbSNPrs754367349
dbSNP (classic)rs754367349
ClinGenrs754367349
ebirs754367349
HLIrs754367349
Exacrs754367349
Gnomadrs754367349
Varsomers754367349
LitVarrs754367349
Maprs754367349
PheGenIrs754367349
Biobankrs754367349
1000 genomesrs754367349
hgdprs754367349
ensemblrs754367349
geneviewrs754367349
scholarrs754367349
googlers754367349
pharmgkbrs754367349
gwascentralrs754367349
openSNPrs754367349
23andMers754367349
23andMe allrs754367349
SNPshotrs754367349
SNPdbers754367349
MSV3drs754367349
GWAS Ctlgrs754367349
Max Magnitude0
ClinVar
Risk rs754367349(-;-)
Alt rs754367349(-;-)
Reference Rs754367349(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RAD51C
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.56787288delT
CLNSRC
CLNACC RCV000484016.1,