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rs149644940

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs149644940(A;C)
Make rs149644940(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome15
Position100573695
GeneLINS1
is asnp
is mentioned by
dbSNPrs149644940
dbSNP (old)rs149644940
ClinGenrs149644940
ebirs149644940
HLIrs149644940
Exacrs149644940
Gnomadrs149644940
Varsomers149644940
Maprs149644940
PheGenIrs149644940
Biobankrs149644940
1000 genomesrs149644940
hgdprs149644940
ensemblrs149644940
gopubmedrs149644940
geneviewrs149644940
scholarrs149644940
googlers149644940
pharmgkbrs149644940
gwascentralrs149644940
openSNPrs149644940
23andMers149644940
23andMe allrs149644940
SNPshotrs149644940
SNPdbers149644940
MSV3drs149644940
GWAS Ctlgrs149644940
Max Magnitude0
ClinVar
Risk rs149644940(C;C)
Alt rs149644940(C;C)
Reference Rs149644940(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LINS LINS1
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.101113900A>C
CLNSRC
CLNACC RCV000397760.1,