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rs1057519172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519172(A;A)
Make rs1057519172(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position37744354
GeneERLIN2
is asnp
is mentioned by
dbSNPrs1057519172
dbSNP (old)rs1057519172
ClinGenrs1057519172
ebirs1057519172
HLIrs1057519172
Exacrs1057519172
Gnomadrs1057519172
Varsomers1057519172
Maprs1057519172
PheGenIrs1057519172
Biobankrs1057519172
1000 genomesrs1057519172
hgdprs1057519172
ensemblrs1057519172
gopubmedrs1057519172
geneviewrs1057519172
scholarrs1057519172
googlers1057519172
pharmgkbrs1057519172
gwascentralrs1057519172
openSNPrs1057519172
23andMers1057519172
23andMe allrs1057519172
SNPshotrs1057519172
SNPdbers1057519172
MSV3drs1057519172
GWAS Ctlgrs1057519172
Max Magnitude0
ClinVar
Risk rs1057519172(A;A)
Alt rs1057519172(A;A)
Reference Rs1057519172(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ERLIN2
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.37601872G>A
CLNSRC
CLNACC RCV000416259.1,