Variant (rsID / SNP)

rs4895441

rs4895441 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LOC105378010. Location: chromosome 6, position 135,426,573. Clinical significance in the table: Benign.

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Reference-table entries

LOC105378010Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:135426573
Cytoband: 6q23.3
HGVS: NC_000006.12:g.135105435A>G

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.