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rs781691587

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs781691587(A;A)
Make rs781691587(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position150558996
GeneADAMTSL4
is asnp
is mentioned by
dbSNPrs781691587
dbSNP (classic)rs781691587
ClinGenrs781691587
ebirs781691587
HLIrs781691587
Exacrs781691587
Gnomadrs781691587
Varsomers781691587
LitVarrs781691587
Maprs781691587
PheGenIrs781691587
Biobankrs781691587
1000 genomesrs781691587
hgdprs781691587
ensemblrs781691587
geneviewrs781691587
scholarrs781691587
googlers781691587
pharmgkbrs781691587
gwascentralrs781691587
openSNPrs781691587
23andMers781691587
23andMe allrs781691587
SNPshotrs781691587
SNPdbers781691587
MSV3drs781691587
GWAS Ctlgrs781691587
Max Magnitude0
ClinVar
Risk rs781691587(A;A)
Alt rs781691587(A;A)
Reference Rs781691587(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ADAMTSL4
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.150531472G>A
CLNSRC
CLNACC RCV000444305.1,