Variant (rsID / SNP)

rs3735644

rs3735644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCC1. Location: chromosome 7, position 127,222,157. The table records no clinical significance for this variant.

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Reference-table entries

GCC1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:127222157
HGVS: NM_024523.6,c.2239C>T,p.Leu747Leu
Allele change: Synonymous_L747L

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.