Variant (rsID / SNP)

rs47

rs47 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to THSD7A. Location: chromosome 7, position 11,581,121. The table records no clinical significance for this variant.

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Reference-table entries

THSD7ANot classified

Variant type: missense_variant
Chromosome / position: 7:11581121
HGVS: NM_015204.3,c.1747A>G,p.Asn583Asp
Allele change: Missense_N583D

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.