Variant (rsID / SNP)

rs16878472

rs16878472 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RASGRF2. Location: chromosome 5, position 80,409,407. The table records no clinical significance for this variant.

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Reference-table entries

RASGRF2Not classified

Variant type: missense_variant
Chromosome / position: 5:80409407
HGVS: NM_006909.3,c.2138T>G,p.Leu713Trp
Allele change: Missense_L713W

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.