Variant (rsID / SNP)

rs7027771

rs7027771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ANKS6. Location: chromosome 9, position 101,552,955. The table records no clinical significance for this variant.

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Reference-table entries

ANKS6Not classified

Variant type: intron_variant
Chromosome / position: 9:101552955
HGVS: NM_173551.5,c.360-67A>G
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.