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Variant (rsID / SNP)

rs13194610

VGLL2

rs13194610 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VGLL2. Location: chromosome 6, position 117,591,755. The table records no clinical significance for this variant.

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Reference-table entries

VGLL2Not classified
Variant type
synonymous_variant
Chromosome / position
6:117591755
HGVS
NM_182645.3,c.441T>C,p.Asn147Asn
Allele change
Synonymous_N147N

Public references

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