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rs1057524695

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057524695(A;T)
Make rs1057524695(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position35831049
GeneNPHS1
is asnp
is mentioned by
dbSNPrs1057524695
dbSNP (old)rs1057524695
ClinGenrs1057524695
ebirs1057524695
HLIrs1057524695
Exacrs1057524695
Gnomadrs1057524695
Varsomers1057524695
Maprs1057524695
PheGenIrs1057524695
Biobankrs1057524695
1000 genomesrs1057524695
hgdprs1057524695
ensemblrs1057524695
gopubmedrs1057524695
geneviewrs1057524695
scholarrs1057524695
googlers1057524695
pharmgkbrs1057524695
gwascentralrs1057524695
openSNPrs1057524695
23andMers1057524695
23andMe allrs1057524695
SNPshotrs1057524695
SNPdbers1057524695
MSV3drs1057524695
GWAS Ctlgrs1057524695
Max Magnitude0
ClinVar
Risk rs1057524695(T;T)
Alt rs1057524695(T;T)
Reference Rs1057524695(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NPHS1
CLNDBN not provided
Reversed 1
HGVS NC_000019.9:g.36321951T>A
CLNSRC
CLNACC RCV000442634.1,