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rs786205624

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205624(C;C)
Make rs786205624(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position74526070
GeneLTBP2
is asnp
is mentioned by
dbSNPrs786205624
ebirs786205624
HLIrs786205624
Exacrs786205624
Varsomers786205624
Maprs786205624
PheGenIrs786205624
hapmaprs786205624
1000 genomesrs786205624
hgdprs786205624
ensemblrs786205624
gopubmedrs786205624
geneviewrs786205624
scholarrs786205624
googlers786205624
pharmgkbrs786205624
gwascentralrs786205624
openSNPrs786205624
23andMers786205624
23andMe allrs786205624
SNP Nexus

SNPshotrs786205624
SNPdbers786205624
MSV3drs786205624
GWAS Ctlgrs786205624
Max Magnitude0
ClinVar
Risk rs786205624(C;C)
Alt rs786205624(C;C)
Reference rs786205624(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LTBP2
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.74992773C>G
CLNSRC
CLNACC RCV000171477.1,