Variant (rsID / SNP)

rs1150781

rs1150781 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMIM29, HMGA1. Location: chromosome 6, position 34,214,322. The table records no clinical significance for this variant.

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Reference-table entries

SMIM29Not classified

Variant type: 3_prime_UTR_variant
Chromosome / position: 6:34214322
HGVS: NM_001008703.4,c.*258G>C
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.