rs145449046

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Rare Variant(gnomAD Genomes)

Snp

Missense

Assembly	Sequence	Position	Alleles	Source
GRCh38	NC_000007.14(opens in new window)	117592541	C > A C > G C > T	dbSnp
GRCh37	NC_000007.13(opens in new window)	117232595	C > A C > G C > T	dbSnp
	NG_016465.4(opens in new window)	131758	C > A C > G C > T	dbSnp
	NP_000483.3(opens in new window)	792	R > * R > G	dbSnp

This variant is considered rare based on global allele frequencies based on data from gnomAD Genomes. more info

PA166394981