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rs72658163

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs72658163(A;A)
Make rs72658163(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position94420276
GeneCHRNA1, COL1A2
is asnp
is mentioned by
dbSNPrs72658163
ebirs72658163
HLIrs72658163
Exacrs72658163
Varsomers72658163
Maprs72658163
PheGenIrs72658163
hapmaprs72658163
1000 genomesrs72658163
hgdprs72658163
ensemblrs72658163
gopubmedrs72658163
geneviewrs72658163
scholarrs72658163
googlers72658163
pharmgkbrs72658163
gwascentralrs72658163
openSNPrs72658163
23andMers72658163
23andMe allrs72658163
SNP Nexus

SNPshotrs72658163
SNPdbers72658163
MSV3drs72658163
GWAS Ctlgrs72658163
Max Magnitude0
OMIM120160
Desc
Variant0020
Relatedalso


ClinVar
Risk rs72658163(A;A)
Alt rs72658163(A;A)
Reference rs72658163(G;G)
Significance Unknown
Disease Marfan syndrome
Variation info
Gene COL1A2
CLNDBN Marfan syndrome, atypical
Reversed 0
HGVS NC_000007.13:g.94049588G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018790.4,