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rs761651320

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs761651320(C;T)
Make rs761651320(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66087368
GeneASL
is asnp
is mentioned by
dbSNPrs761651320
dbSNP (classic)rs761651320
ClinGenrs761651320
ebirs761651320
HLIrs761651320
Exacrs761651320
Gnomadrs761651320
Varsomers761651320
LitVarrs761651320
Maprs761651320
PheGenIrs761651320
Biobankrs761651320
1000 genomesrs761651320
hgdprs761651320
ensemblrs761651320
geneviewrs761651320
scholarrs761651320
googlers761651320
pharmgkbrs761651320
gwascentralrs761651320
openSNPrs761651320
23andMers761651320
23andMe allrs761651320
SNPshotrs761651320
SNPdbers761651320
MSV3drs761651320
GWAS Ctlgrs761651320
Max Magnitude0
ClinVar
Risk rs761651320(T;T)
Alt rs761651320(T;T)
Reference Rs761651320(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ASL
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.65552355C>T
CLNSRC
CLNACC RCV000489563.1,