Variant (rsID / SNP)

rs7307331

rs7307331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VSIG10. Location: chromosome 12, position 118,509,191. The table records no clinical significance for this variant.

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Reference-table entries

VSIG10Not classified

Variant type: missense_variant
Chromosome / position: 12:118509191
HGVS: NM_019086.6,c.1303C>T,p.His435Tyr
Allele change: Missense_H435Y

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.