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rs797044888

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044888(G;T)
Make rs797044888(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position46267600
GeneRAD54L
is asnp
is mentioned by
dbSNPrs797044888
ebirs797044888
HLIrs797044888
Exacrs797044888
Varsomers797044888
Maprs797044888
PheGenIrs797044888
hapmaprs797044888
1000 genomesrs797044888
hgdprs797044888
ensemblrs797044888
gopubmedrs797044888
geneviewrs797044888
scholarrs797044888
googlers797044888
pharmgkbrs797044888
gwascentralrs797044888
openSNPrs797044888
23andMers797044888
23andMe allrs797044888
SNP Nexus

SNPshotrs797044888
SNPdbers797044888
MSV3drs797044888
GWAS Ctlgrs797044888
Max Magnitude0
ClinVar
Risk rs797044888(T;T)
Alt rs797044888(T;T)
Reference rs797044888(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RAD54L
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000001.10:g.46733272G>T
CLNSRC
CLNACC RCV000190710.1,