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Variant (rsID / SNP)

rs4971432

SNTG2

rs4971432 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SNTG2. Location: chromosome 2, position 1,079,320. The table records no clinical significance for this variant.

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Reference-table entries

SNTG2Not classified
Variant type
synonymous_variant
Chromosome / position
2:1079320
HGVS
NM_018968.4,c.189C>T,p.Gly63Gly
Allele change
Synonymous_G63G

Public references

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