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rs1057517993

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057517993(-;C)
Make rs1057517993(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position2249540
GeneAMH, MIR4321
is asnp
is mentioned by
dbSNPrs1057517993
dbSNP (old)rs1057517993
ClinGenrs1057517993
ebirs1057517993
HLIrs1057517993
Exacrs1057517993
Gnomadrs1057517993
Varsomers1057517993
Maprs1057517993
PheGenIrs1057517993
Biobankrs1057517993
1000 genomesrs1057517993
hgdprs1057517993
ensemblrs1057517993
gopubmedrs1057517993
geneviewrs1057517993
scholarrs1057517993
googlers1057517993
pharmgkbrs1057517993
gwascentralrs1057517993
openSNPrs1057517993
23andMers1057517993
23andMe allrs1057517993
SNPshotrs1057517993
SNPdbers1057517993
MSV3drs1057517993
GWAS Ctlgrs1057517993
Max Magnitude0
ClinVar
Risk rs1057517993(C;C)
Alt rs1057517993(C;C)
Reference Rs1057517993(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene AMH MIR4321
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.2249539dupC
CLNSRC
CLNACC RCV000414343.1,