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rs757318536

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs757318536(C;T)
Make rs757318536(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position150553240
GeneADAMTSL4, LOC100289061
is asnp
is mentioned by
dbSNPrs757318536
dbSNP (classic)rs757318536
ClinGenrs757318536
ebirs757318536
HLIrs757318536
Exacrs757318536
Gnomadrs757318536
Varsomers757318536
LitVarrs757318536
Maprs757318536
PheGenIrs757318536
Biobankrs757318536
1000 genomesrs757318536
hgdprs757318536
ensemblrs757318536
geneviewrs757318536
scholarrs757318536
googlers757318536
pharmgkbrs757318536
gwascentralrs757318536
openSNPrs757318536
23andMers757318536
23andMe allrs757318536
SNPshotrs757318536
SNPdbers757318536
MSV3drs757318536
GWAS Ctlgrs757318536
Max Magnitude0
ClinVar
Risk rs757318536(T;T)
Alt rs757318536(T;T)
Reference Rs757318536(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ADAMTSL4 LOC100289061
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.150525716C>T
CLNSRC
CLNACC RCV000440699.1,