Variant (rsID / SNP)

rs6905572

rs6905572 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MSH5, VWA7. Location: chromosome 6, position 31,731,881. Clinical significance in the table: Benign.

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Reference-table entries

MSH5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:31731881
Cytoband: 6p21.33
HGVS: NM_001039651.2(SAPCD1):c.296C>T (p.Pro99Leu)
Allele change: Silent

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.