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rs148606936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148606936(A;A)
Make rs148606936(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152303434
GeneFLG
is asnp
is mentioned by
dbSNPrs148606936
dbSNP (old)rs148606936
ClinGenrs148606936
ebirs148606936
HLIrs148606936
Exacrs148606936
Gnomadrs148606936
Varsomers148606936
Maprs148606936
PheGenIrs148606936
Biobankrs148606936
1000 genomesrs148606936
hgdprs148606936
ensemblrs148606936
gopubmedrs148606936
geneviewrs148606936
scholarrs148606936
googlers148606936
pharmgkbrs148606936
gwascentralrs148606936
openSNPrs148606936
23andMers148606936
23andMe allrs148606936
SNPshotrs148606936
SNPdbers148606936
MSV3drs148606936
GWAS Ctlgrs148606936
Max Magnitude0
ClinVar
Risk rs148606936(A;A) rs148606936(T;T)
Alt rs148606936(A;A) rs148606936(T;T)
Reference Rs148606936(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152275910G>A
CLNSRC
CLNACC RCV000365311.1,