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rs483353128

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs483353128(A;A)
Make rs483353128(A;C)
ReferenceGRCh38 38.1/142
Chromosome4
Position173528900
GeneHAND2, HAND2-AS1
is asnp
is mentioned by
dbSNPrs483353128
ebirs483353128
HLIrs483353128
Exacrs483353128
Varsomers483353128
Maprs483353128
PheGenIrs483353128
hapmaprs483353128
1000 genomesrs483353128
hgdprs483353128
ensemblrs483353128
gopubmedrs483353128
geneviewrs483353128
scholarrs483353128
googlers483353128
pharmgkbrs483353128
gwascentralrs483353128
openSNPrs483353128
23andMers483353128
23andMe allrs483353128
SNP Nexus

SNPshotrs483353128
SNPdbers483353128
MSV3drs483353128
GWAS Ctlgrs483353128
Max Magnitude0
ClinVar
Risk rs483353128(A;A)
Alt rs483353128(A;A)
Reference rs483353128(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HAND2-AS1 HAND2
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.174450051G>T
CLNSRC ClinVar
CLNACC RCV000128538.1,