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rs370356566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs370356566(A;A)
Make rs370356566(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position157471733
GeneNIPAL4
is asnp
is mentioned by
dbSNPrs370356566
dbSNP (classic)rs370356566
ClinGenrs370356566
ebirs370356566
HLIrs370356566
Exacrs370356566
Gnomadrs370356566
Varsomers370356566
LitVarrs370356566
Maprs370356566
PheGenIrs370356566
Biobankrs370356566
1000 genomesrs370356566
hgdprs370356566
ensemblrs370356566
geneviewrs370356566
scholarrs370356566
googlers370356566
pharmgkbrs370356566
gwascentralrs370356566
openSNPrs370356566
23andMers370356566
23andMe allrs370356566
SNPshotrs370356566
SNPdbers370356566
MSV3drs370356566
GWAS Ctlgrs370356566
Max Magnitude0
ClinVar
Risk rs370356566(A;A)
Alt rs370356566(A;A)
Reference Rs370356566(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ADAM19 NIPAL4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.156898741G>A
CLNSRC
CLNACC RCV000414650.1,